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Assistant Project Manager – Longitudinal Study Of Health And Ageing In Kenya (Loshak)

Department: Population Health
Division: Medical College
Location: Nairobi, Kenya

Job Summary

LOSHAK (Longitudinal Study of Health and Ageing in Kenya) is a major research collaboration between the Aga Khan University in Nairobi and the University of Michigan, involving multiple Kenyan and international partners including Kenya’s Ministry of Health and National Bureau of Statistics. Funded by the U.S. National Institute on Aging, this project will collect multi-modal data (surveys, biological measures, mobile health assessments, etc.) from over 8,000 older Kenyans, examining nearly all aspects of their physical, cognitive, psychosocial, and economic well-being. LOSHAK is also part of a large global network of harmonized aging studies modeled on the U.S. Health and Retirement Study, with the aim of informing public health policy and improving the well-being of older populations in Kenya and beyond.

As the Assistant Project Manager, you will work within the Department of Population Health at Aga Khan University (Nairobi) and report directly to the LOSHAK Project Manager. In this supportive role, you will help coordinate all aspects of the project’s implementation – from planning and budgeting to fieldwork management, stakeholder coordination, and reporting – to ensure the study’s objectives are met on time and with high quality. This position requires excellent organizational and communication skills, as you will act as a key liaison among the project’s multidisciplinary team and external collaborators. You will be responsible for maintaining smooth day-to-day operations in support of the Project Manager and the Kenya Principal Investigator, helping to advance LOSHAK’s mission and research goals.

Key Responsibilities

Project Planning And Coordination

Work closely with the LOSHAK Project Manager and U.S.-based counterparts to coordinate the implementation of all study aims, supporting project management activities across all dimensions of the study.
Assist in project planning and administration, including contributing to budgeting, developing work plans, scheduling field implementation, coordinating stakeholders, managing procurement processes, and preparing project reports.
Coordinate logistical arrangements for internal project activities, such as scheduling team meetings, organizing interviewer training sessions, and supporting study pre-tests and pilot field activities for the Kenya-based team.

Stakeholder Engagement And Communication

Facilitate collaboration among LOSHAK co-investigators and subject-matter experts by organizing meetings/workshops to develop and refine survey modules in each investigator’s area of expertise.
Liaise with external project partners (across local and international institutions) under the guidance of the Project Manager to ensure smooth implementation of project activities and to help identify any needed adjustments in project plans.
Support the Project Manager in engaging with key stakeholders – including NGOs, academic partners, and government agencies – to foster dialogue, knowledge exchange, and effective policy engagement around ageing and health issues.

Monitoring And Reporting

Work with local and international collaborators on the data management team to ensure timely data processing and the generation of quality assurance reports for the study.
Monitor project timelines and milestones, proactively identifying potential delays or issues, and provide regular progress updates to the Project Manager and study leadership.
Assist in preparing required progress reports and documentation for project stakeholders (partners and funders), ensuring that reporting requirements and deadlines are fully met.
Work closely with the grants and finance administrative staff to track project expenditures and monitor grant spending, helping to ensure budget compliance and efficient use of resources.

Administrative Support And Other Duties

Provide administrative support for project human resources, including coordinating the recruitment and onboarding of PhD students and post-doctoral fellows, and facilitating their ongoing involvement and support within the project.
Maintain flexibility in work hours, with willingness to adjust to early-morning or late-evening calls as needed to accommodate collaborators in different time zones.
Be prepared to travel domestically within Kenya and internationally for project meetings, training sessions, or field oversight, as required by the project.
Perform other duties or special projects as assigned by the LOSHAK Project Manager or study leadership, in line with the evolving needs of the project.

Required Qualifications

Bachelor’s degree in a relevant field (e.g. public health, population health, social sciences, business or related discipline) with at least 3 years of relevant project management/coordination experience, OR a Master’s degree in a relevant field with 1–2 years of experience in project coordination.
Excellent organizational and time-management skills, including the ability to effectively manage multiple tasks or projects simultaneously while maintaining a high level of attention to detail.
Demonstrated ability to work productively under pressure and meet deadlines in a fast-paced environment.
High degree of initiative, resourcefulness, and self-direction, with strong analytical and problem-solving abilities. Ability to exercise sound judgment in troubleshooting issues, and to know when to escalate problems or seek guidance appropriately.
Excellent verbal and written communication skills, with the ability to interact professionally with diverse teams and stakeholders at all levels. Strong interpersonal skills and the ability to collaborate effectively with colleagues from varied backgrounds in Kenya and internationally.
Proficiency in standard office and project management software tools, including Microsoft Office (Word, Excel, PowerPoint) and email/calendar applications. Familiarity with online survey and data collection tools (such as Qualtrics or Google Forms) and videoconferencing platforms (e.g. Zoom) is highly desirable.
Demonstrated reliability, integrity, and accountability in previous roles. A strong work ethic with a proactive attitude, flexibility, and resilience in facing challenges. Ability to maintain confidentiality and handle sensitive information with discretion and professionalism.

Preferred Qualifications

Academic/Research Environment Experience: Knowledge of or experience with university or research institution procedures and regulations, such as familiarity with research ethics committees, grant administration, or academic program operations.
Project Experience in LMICs: Prior involvement in health or social research projects in low- or middle-income country settings (especially in Kenya or Sub-Saharan Africa). Experience supporting or implementing projects focused on public health or ageing populations in these contexts is an advantage.

Primary Location

: Kenya-Nairobi

Organisation

: Aga Khan University Hospital Kenya

Employee Status

: Regular

Job Type

: Experienced

Job Posting

: 19/09/2025, 7:17:58 AM

Closing Date

: 03/10/2025, 6:59:00 PM","hiringOrganization":{"@type":"Organization","name":"Aga Khan University","sameAs":"https://www.aku.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Kenya-Nairobi","addressCountry":"Kenya","addressRegion":"Africa"}}}},{"@type":"ListItem","position":2,"item":{"@type":"JobPosting","title":"Project Manager, Population Health","datePosted":"2025-09-19","description":"Project Manager, Population Health - (250002P1)

Project Manager – Longitudinal Study of Health and Ageing in Kenya (LOSHAK)
Department: Population Health
Division: Medical College
Location: Nairobi, Kenya

Job Summary

The Longitudinal Study of Health and Ageing in Kenya (LOSHAK) is a multidisciplinary study that aims to collect data on health and economic wellbeing in later-life in Kenya. LOSHAK is a collaboration between the Aga Khan University - Nairobi and the University of Michigan - US along with collaborators across universities in the US and Kenya, The Kenya Ministry of Health, the Kenya National Bureau of Statistics, and the KEMRI Air Pollution Centre of Excellence. The project, funded by the National Institutes of Health, will collect multimodal data (surveys, biomarkers, mobile wearables and health measures) from more than 8,000 older Kenyans, touching on nearly all aspects of physical, psychosocial, cognitive, and economic wellbeing. LOSHAK is part of large global networks of harmonized studies focused on late-life health and economic wellbeing (The Health and Retirement Studies Around the World Network and The Harmonized Cognitive Protocol Assessment Network). This study aims to inform public policy and public health planning in Kenya and neighboring countries, all of which are experiencing rapid population aging.

Working under the supervision of the Kenya LOSHAK Principal Investigator, this individual will help to advance LOSHAK’s scientific aims, which include: collecting population-representative data on older adults’ health and economic wellbeing, making data publicly available to the research community, and strengthening research capacity in Kenya. This individual will lead efforts to design, develop, and execute LOSHAK’s aims from the outset of the project, and will therefore play a critical role on the large and multidisciplinary project team. Strong emphasis will be placed on developing tactics to ensure timely, coordinated, and high-quality workflows across the large team.

Responsibilities

The Project Manager will work with a US-based counterpart to manage implementation of LOSHAK study aims and will have responsibility for project management across all dimensions of the study.
Lead all the project planning and administrative functions including budgeting, work planning, field implementation, collaborator and stakeholder coordination, procurement and reporting among others.
Convene LOSHAK collaborators/co-investigators to develop survey modules in their areas of expertise.
Work closely with local and international LOSHAK collaborators to ensure timely data management and report generation for quality assurance.
Interface with partners to ensure smooth implementation and identify when changes need to be made.
Conduct project meetings, track and analyze project progress, report on progress to study leadership.
Prepare progress reports for partners and funders as needed.
Support dialogue and education between NGOs, academia and government offices to ensure effective and efficient policy engagement.
Assist the Kenya-based team with planning team meetings, interviewer trainings, and study pretest and pilot activities.
Work with grants and finance administrative staff to monitor grant spending.
Manage PhD students and post-doc recruitment and support.
If/as needed, willingness to engage in a flexible work schedule to attend early morning meetings and/or late meetings and events to accommodate colleagues in diverse time zones
Other responsibilities and/or projects as assigned by the study leadership
International travel as needed

Required Qualifications

Master’s degree in public health, public policy, business, or other related field, and five years or more of professional project management experience.
Outstanding organizational skills and ability to effectively manage numerous projects, simultaneously and in various stages of development, with a high attention to detail.
Ability to analyze, compare and evaluate various courses of action and make independent decisions on matters of significance, free from immediate direction within the scope of job responsibilities, ability to manage multiple and competing priorities.
Must have strong integrity, be highly proactive, have a high degree of problem-solving skills, be highly reliable, retain a sense of ownership and accountability for workload, be flexible and resilient, provide excellent customer service, and possess expert follow-up skills.
Possess excellent written and verbal communication skills and ability to interact with and build professional relationships with all individuals at all levels; appropriately handle confidential and sensitive information.
Proficient computer skills are essential, including demonstrated proficiency with Outlook, Word, Excel, PowerPoint, Adobe PDFs, survey tools such as Qualtrics and Google Forms, and Zoom.
Must be productive and flexible under pressure and able to meet deadlines.

Desired Qualifications

Knowledge of University or Research Institution environments, practices, rules and regulations.
Previous experience leading the implementation of health projects in Low- or Middle-Income Countries (LMICs).

Primary Location

: Kenya-Nairobi

Organisation

: Aga Khan University Hospital Kenya

Employee Status

: Regular

Job Type

: Experienced

Job Posting

: 19/09/2025, 7:19:52 AM

Closing Date

: 03/10/2025, 6:59:00 PM","hiringOrganization":{"@type":"Organization","name":"Aga Khan University","sameAs":"https://www.aku.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Kenya-Nairobi","addressCountry":"Kenya","addressRegion":"Africa"}}}},{"@type":"ListItem","position":3,"item":{"@type":"JobPosting","title":"Research Associate, Population Health","datePosted":"2025-09-19","description":"Research Associate, Population Health - (250002P4)

Research Associate – Longitudinal Study Of Health And Ageing In Kenya (Loshak)

Department: Population Health
Division: Medical College
Location: Nairobi, Kenya

Project Overview

The Longitudinal Study of Health and Ageing in Kenya (LOSHAK) is a national research initiative examining the health, economic, social, and environmental factors affecting Kenya’s rapidly growing older adult population. Modeled on the U.S. Health and Retirement Study, LOSHAK will collect and disseminate high-quality data harmonized with global aging studies in over 45 countries. The project’s mission is to inform public health policy and improve the health, economic circumstances, and wellbeing of older Kenyans. This study is implemented by the Department of Population Health at Aga Khan University in collaboration with international partners and supported by the National Institute on Aging of the National Institute of Health, US.

Role Summary

We are seeking a highly motivated post-doctoral Research Associate to lead and support key research activities for the LOSHAK project. The Research Associate will play a central role in study protocol development, regulatory approvals, data management and analysis, manuscript preparation, field coordination, stakeholder engagement, and overall quality control of the study. The ideal candidate is a recent PhD graduate in a health-related field (e.g. Public Health, Epidemiology, Population Health) with strong research methodology skills and some postdoctoral research experience. This is a full-time, five-year position in which the incumbent will work under the supervision of the LOSHAK Principal Investigator to ensure the study’s successful implementation and scientific excellence. This position offers a unique opportunity to contribute to groundbreaking research on ageing in Africa. The successful candidate will gain experience in all phases of the research process – from conception to dissemination – and work closely with leading experts at Aga Khan University and the University of Michigan. The role is ideal for a recent PhD graduate looking to build an academic career in population health research while making a meaningful impact on policy and practice.

Key Responsibilities

Study Design & Protocol Development: Contribute to study conceptualization and design, including drafting and refining research protocols and instruments to meet the project’s objectives. Prepare documentation for Institutional Scientific and Ethics Review Committee (ISERC) submissions, and ensure all regulatory approvals are obtained and maintained throughout the project lifespan.
Project Coordination: Coordinate the day-to-day implementation of the project to meet milestones and timelines. This includes developing fieldwork plans, scheduling and supervising data collection activities, and monitoring project progress against targets. Ensure smooth collaboration across the multi-disciplinary project team (local and international) and proactively identify and resolve operational challenges.
Development of Research Tools & SOPs: Lead the development and refinement of data collection tools (surveys, interview guides, assessment forms) and Standard Operating Procedures (SOPs) for all aspects of study implementation. Continuously update study protocols and SOPs as needed to reflect best practices and lessons learned during the project.
Field Staff Training & Supervision: Oversee the recruitment, training, and supervision of field staff, including enumerators, interviewers, and other research assistants and students. Develop training manuals and conduct training sessions to ensure field teams are well-versed in study procedures, ethical research conduct, and data collection techniques. Provide ongoing mentorship and support to field teams and enforce adherence to study protocols during fieldwork.
Data Management & Quality Control: Working with the data team, support the establishment and management of robust data management processes for the project. Oversee data collection, entry, cleaning, and secure storage of study data. Ensure data quality by implementing real-time quality checks, field monitoring visits, and periodic audits of collected data. Follow and enforce all project-related SOPs and guidelines during field implementation and take corrective action to address any deviations.
Data Analysis & Interpretation: Work with LOSHAK statisticians to conduct statistical data analyses using appropriate software (e.g. Stata, R) to answer the study’s research questions. Work with the investigative team to interpret results in the context of existing evidence and the Kenyan setting. Apply rigorous research methods and, where appropriate, novel analytical approaches to generate high-quality findings.
Reporting & Documentation: Support the preparation of regular project progress reports and updates for the Principal Investigator, funders, and other stakeholders. Document all research activities thoroughly, including maintaining records of data collection, training, and any protocol amendments. Assist in preparing technical reports and grant reports as required.
Manuscript Writing & Publication: Lead and contribute to the writing of scientific manuscripts to publish the study’s findings in peer-reviewed journals. Conduct literature reviews and collaborate with co-investigators to frame the study results within the broader scientific literature. Take primary responsibility for drafting manuscripts, incorporating co-authors’ inputs, and managing the submission and revision process with journals.
Stakeholder Engagement & Dissemination: Engage with a range of stakeholders at various stages of the project to ensure its success and impact. Liaise with community leaders, local health officials, and district stakeholders to gain community entry and support for field activities. Work with national and international collaborators (including the University of Michigan team) to harmonize study protocols and share learnings. Participate in disseminating research findings to appropriate audiences – including policymakers, academic conferences, and community forums – and lead the preparation of policy briefs and presentations to translate findings into actionable insights.
Quality Assurance: Uphold the highest standards of research ethics and integrity throughout the project. Ensure compliance with all institutional and national research regulations (e.g., obtaining renewals of ethics approvals, adhering to data protection and privacy laws). Continuously monitor study processes for potential issues or biases and implement improvements to maintain scientific rigor.

Qualifications And Experience

Education: PhD in Public Health, Epidemiology, Biostatistics, Population Health, or a related health sciences field. The candidate should have strong training in research methods and study design relevant to population health research.
Research Experience: A minimum of 2 years of relevant research experience post-PhD, preferably including involvement in large-scale field research or longitudinal studies. Experience in health or demographic research (especially on ageing or non-communicable diseases) in sub-Saharan Africa is highly desirable.
Data Analysis Skills: Proven skills in quantitative data management and analysis, including proficiency in statistical software such as Stata, R or Python. Ability to manage and analyze large datasets and perform advanced statistical analyses is required. Familiarity with qualitative research methods and mixed-methods analysis is an added advantage.
Publication Track Record: A strong record of scholarly output, evidenced by peer-reviewed publications or conference presentations in relevant topics. Excellent scientific writing and literature review skills are essential.
Project Management & Coordination Skills: Demonstrated ability to manage research projects or significant components thereof – from protocol development and ethics submissions to field implementation and team coordination. Experience developing research instruments and overseeing data collection in community settings is highly valued.
Leadership & Teamwork: Excellent organizational and leadership skills, including the ability to supervise and motivate field teams, manage multiple tasks simultaneously, and meet deadlines. Capacity to work independently with minimal supervision, as well as effectively as part of a multidisciplinary, multicultural team.
Communication & Interpersonal Skills: Strong interpersonal skills and the ability to communicate effectively with diverse stakeholders – from community members to academic partners. Proficiency in English (written and oral) is required, with superb report writing and presentation skills. Knowledge of Kiswahili or other local languages is an asset for community engagement (though not mandatory).
Ethical and Regulatory Knowledge: Familiarity with research ethics processes and regulations in Kenya (or similar contexts), including experience preparing IRB applications and ensuring compliance with human subjects protections. A thorough understanding of data security and confidentiality practices.
Flexibility & Commitment: Willingness to travel within Kenya to oversee fieldwork activities as needed, including to rural or remote areas. Ability to adapt to dynamic field conditions and work under pressure while maintaining attention to detail. A strong work ethic, professional integrity, and passion for improving health outcomes for older populations.

Primary Location

: Kenya-Nairobi

Organisation

: Aga Khan University Hospital Kenya

Employee Status

: Regular

Job Type

: Experienced

Job Posting

: 19/09/2025, 7:21:05 AM

Closing Date

: 03/10/2025, 6:59:00 PM","hiringOrganization":{"@type":"Organization","name":"Aga Khan University","sameAs":"https://www.aku.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Kenya-Nairobi","addressCountry":"Kenya","addressRegion":"Africa"}}}},{"@type":"ListItem","position":4,"item":{"@type":"JobPosting","title":"Clinical Research Associate II","datePosted":"2025-09-19","description":"Clinical Research Associate II

Required Qualifications (as evidenced by an attached resume):
Bachelor's Degree in appropriate field. Three (3) years of full-time research experience. Two (2) years of full-time patient-facing clinical trials research experience involving interventional studies (drug or device). Experience working with Electronic Health Records for inclusion/exclusion criteria and consenting research subjects.

Preferred Qualifications:

Five (5) or more years’ experience in clinical trials and regulatory compliance. Bilingual in English and Spanish. Phlebotomy experience. Experience in processing human samples.

Brief Description of Duties:
Ensure smooth, accurate progress of the clinical trial from planning stage through trial completion and post study closure by working with the investigator, human subjects, Institutional Review Board, university and sponsor. Incumbent works independently with general direction from the Principal Investigator and performs complex and interrelated tasks for multiple studies.

Duties:

Coordinate various research trials and ensure compliance with federal guidelines.
Screen, consent, and enroll patients for clinical research trials; complete study patient visits; collect, enter, and submit clinical trial patient data.
Collection, processing, and shipment of human blood samples and biospecimens
Administrative duties such as billing, budgeting, and contract administration; maintenance of clinical research study supplies and drug accountability.
Interact and correspond with various internal and external constituents including sponsors, cooperative groups, Institutional Review Board and regulatory agencies.
Assist principal investigators with grant submissions and renewals.
May supervise or coordinate the work of other staff.
Other duties as assigned.

Special Notes:
The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption.

Essential Position: This has been designated as an essential position based on the duties of the job and the functions performed. Positions that are designated as such may be required to report to work/remain at work even if classes are canceled, and the campus is working on limited operations in an emergency.

For this position, we are unable to sponsor candidates for work visas.

Resume/CV and cover letter should be included with the online application.

Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws.

If you need a disability-related accommodation, please call the university Office of Equity and Access (OEA) at (631) 632-6280 or visit OEA.

In accordance with the Title II Crime Awareness and Security Act a copy of our crime statistics can be viewed here.

Visit our WHY WORK HERE page to learn about the total rewards we offer.

SUNY Research Foundation: A Great Place to Work.

The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU’s good faith and reasonable estimate of the range of possible compensation at the time of posting.

Job Number:

2503665Official Job Title: Clinical Research Associate II

Job Field

: Research Professional / Technical

Primary Location

: US-NY-Stony BrookDepartment/Hiring Area: Office of Scientific Affairs

Schedule

: Full-time

Shift

:Day Shift Shift Hours: 8:30am - 5:00pm

Posting Start Date

: Sep 18, 2025

Posting End Date

: Oct 19, 2025, 3:59:00 AMSalary:$64,000-$83,000Appointment Type: RegularSalary Grade:E99SBU Area:The Research Foundation for The State University of New York at Stony Brook","hiringOrganization":{"@type":"Organization","name":"Stony Brook University","sameAs":"https://www.stonybrook.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US-NY-Stony Brook","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":5,"item":{"@type":"JobPosting","title":"Sr. Research Associate, Pediatrics","datePosted":"2025-09-19","description":"Sr. Research Associate, Pediatrics - (894471)

Description

WHY UT SOUTHWESTERN?
With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!

JOB SUMMARY
Works under minimal direction to plan, coordinate, perform, and supervise performance of professional level medical or scientific research assignment related to particular or specialized field of endeavor.

This position will lead scientific projects and mentor junior scientists; perform a variety of laboratory techniques including but not limited to mammalian cell culture, cloning, nucleic acid extraction, PCR, qRT-PCR, immunoblotting, and immunohistochemistry; record and maintain an organized lab notebook; present findings in small group meetings and at national and international meetings when appropriate.

BENEFITS
UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

PPO medical plan, available day one at no cost for full-time employee-only coverage
100% coverage for preventive healthcare-no copay
Paid Time Off, available day one
Retirement Programs through the Teacher Retirement System of Texas (TRS)
Paid Parental Leave Benefit
Wellness programs
Tuition Reimbursement
Public Service Loan Forgiveness (PSLF) Qualified Employer
Learn more about these and other UTSW employee benefits!

Experience And Educationrequired

EducationPhD with major coursework in field of assignment and no experience or Master's Degree with major coursework in field of assignment or Bachelor's Degree with major coursework in field of assignment or
ExperienceNo experience required with PhD or 5 years of laboratory experience with a Master's Degree including at least 2 years at level of Research Associate or equivalent or 6 years of laboratory experience with a Bachelor's Degree including at least 2 years at level of Research Associate or equivalent

Job Duties

Organizes laboratory to which assigned; determines work assignments of subordinates, advising them as to techniques, procedures, and equipment to be utilized in solution of work problems; reviews completed work for professional quality and attainment of desired results.
Compiles and evaluates research data, and develops new or revised techniques and procedures based upon such data.
Performs or supervises design, development, or adaptation of equipment or apparatus used in experiments or research to obtain desired results.
Compiles and analyzes results of research assignments and submits to principal investigator.
Instructs medical students, graduate students, residents, and other laboratory personnel of lower grade with respect to techniques, procedures, and equipment utilized in research or experiments.
Confers with industrial, governmental, or other professional groups with respect to progress or results of research assignment.
Assists principal investigator and other professional personnel in preparation of reports and papers for publication, usually exercising responsibility for writing of particular segment or phase of report or paper.
Performs other duties as assigned.

SECURITY AND EEO STATEMENT

Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.

EEO
UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.

Primary Location

: Texas-Dallas-5323 Harry Hines Blvd

Work Locations

: 5323 Harry Hines Blvd 5323 Harry Hines Blvd Dallas 75390

Job

: Research & Laboratory

Organization

: 423003 - PD-Cardiology

Schedule

: Full-time

Shift

: Day Job

Employee Status

: Regular

Job Type

: Standard

Job Posting

: Sep 18, 2025, 2:12:43 PM","hiringOrganization":{"@type":"Organization","name":"UT Southwestern Medical Center","sameAs":"https://www.utsouthwestern.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Texas-Dallas-5323 Harry Hines Blvd","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":6,"item":{"@type":"JobPosting","title":"Senior Clinical Research Associate","datePosted":"2025-09-19","description":"

Summary

The Department of Medicine, Section of Gastroenterology & Hepatology at Baylor College of Medicine is seeking a dedicated and reliable Senior Clinical Research Associate to support the day-to-day operations of research projects led by Dr. Othman.

\n\n

The successful candidate will be responsible for managing daily project activities, designing and maintaining study databases, and overseeing participant recruitment across multiple research studies. Additional responsibilities include ensuring regulatory and institutional compliance, maintaining documentation, and supporting reporting requirements for grants and protocols.

\n\n

The ideal candidate is self-motivated, highly organized, and possesses strong leadership skills. This is a full-time position, Monday through Friday, with a 40-hour work week.

Job Duties

Oversees daily operational activities to support productivity and collaboration across multi-site study teams.
Leads coordination of weekly team meetings by setting agendas, facilitating discussions, and synthesizing site reports.
Directs task delegation to study staff—including recruitment, data collection, and compliance activities—while tracking completion.
Guides research team members through training on data systems and protocol adherence; provides support during coordinator meetings.
Oversees participant recruitment and enrollment across multiple sites in alignment with regulatory and protocol standards.
Provides oversight in the use of electronic medical record systems such as EPIC and CPRS for participant screening and tracking.
Maintains responsibility for participant tracking logs and engagement activities.
Designs and maintains study databases tailored to protocol and sponsor specifications.
Prepares and submits IRB amendments, renewals, and protocol updates for regulatory review.
Ensures distribution of regulatory approvals and compliance documentation to all participating sites.
Prepares and submits required documents to Baylor College of Medicine.
Maintains all essential study records, including regulatory binders, correspondence, and audit documentation.
Prepares teams and documentation for monitoring visits and audit reviews.
Ensures secure and timely archiving of all study materials.
Performs other job-related duties as assigned.

Minimum Qualifications

Bachelor's degree.
Four years of relevant experience.

Preferred Qualifications

Master of Science or Medical Degree.
Experience as a Clinical Research Associate (CRA).

\n\n\n

Work Authorization Requirement:

Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment. This position is not eligible for visa sponsorship.

\n\n

Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.

","hiringOrganization":{"@type":"Organization","name":"Baylor College of Medicine","sameAs":"https://www.bcm.edu"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Houston, TX, US","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":7,"item":{"@type":"JobPosting","title":"Research Associate (Structural Biology)","datePosted":"2025-09-19","description":"

School of Molecular Sciences

Full-time appointment on a fixed term basis for two years.
Base salary range: Level A, Step 8, $112,371 p.a. plus 17% superannuation.

About The Area

The School of Molecular Sciences is home to the Structural Biology group of Prof Charlie Bond, alongside colleagues in chemistry, biochemistry and genetics, including Prof Ian Small. The Bond and Small groups collaborate on an Australian Research Council Discovery Project on structure-function studies of pentatricopeptide repeat proteins, an area where they have had consistent national competitive grant funding for 13 years.

The School is located in the Bayliss Building, on the main Crawley campus of the University of Western Australia, a purpose built facility with state of the art research infrastructure for all aspects of molecular sciences based research. The campus is located in Perth, Western Australia, one of the most liveable cities on the planet.

About The Opportunity

Design, overexpress, purify, and structurally analyse variant pentatricopeptide repeat proteins for controlled enzymatic RNA modification using cryo electron microscopy and crystallography.
Work closely with project members on experimental design, data interpretation, and supervise students on a day-to-day basis.
Collaborate with staff at the Centre for Microscopy and Analysis and actively participate in the CryoEM User Group.

About You

A PhD in Structural Biology or a related discipline.
Expertise in standard molecular biology and recombinant protein expression and purification methods.
Expertise in sample preparation, data collection and structure analysis using cryoelectron microscopy (single particle analysis).
Track record (relative to opportunity) of reporting research as evidenced by peer reviewed journal articles published in respected scholarly journals.
Ability to work both independently and as part of an inclusive collaborative team.

Position description: PD [Research Associate (Structural Biology)] [521306].pdf

To learn more about this opportunity, please contact Professor Charlie Bond at charles.bond@uwa.edu.au

How To Apply

Please apply online via the Apply Now button and address the selection criteria in your submission in a separate document. For information to assist you with compiling statements to answer the selection criteria, please visit Addressing the selection criteria.

Closing date: 11:55 PM AWST on Monday, 27 October 2025

This position is open to international applicants.

About The University

The University of Western Australia (UWA) is ranked among the top 100 universities in the world and a member of the prestigious Australian Group of Eight research intensive universities. With a strong research track record, vibrant campus and working environments, supported by the freedom to innovate and inspire, there is no better time to join Western Australia’s top university.

Learn more about us.

Our commitment to inclusion and diversity

UWA is committed to a diverse workforce and an equitable and inclusive workplace. We are committed to fostering a safe environment for all, including Aboriginal and Torres Strait Islander people, women, those from culturally and linguistically diverse backgrounds, the LGBTIQA+ community, and people living with disability.

If you require any reasonable adjustments, we encourage you to advise us at the time of application. Alternatively, you can contact us for assistance during the recruitment process.

\n\n

If you have queries relating to your application, please contact the individual named in the advertisement. Alternatively, please contact the Talent team at people@uwa.edu.au with details of your query. To enable a quick response, please include the 6-digit job reference number.

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About Euromonitor:

Euromonitor International leads the world in data analytics and research into markets, industries, economies and consumers. We provide truly global insight and data on thousands of products and services; we are the first destination for organisations seeking growth. With our guidance, our clients can make bold, strategic decisions with confidence.

About The Role:

As a Project Delivery Research Associate, you will play a pivotal role in transforming complex data into actionable insights. You’ll harness large-scale datasets, utilize key secondary sources, and apply rigorous research methodologies to construct and validate quantitative models. This process involves standardizing data collection and analysis techniques to ensure transparency, consistency, and efficiency across projects. You’ll be expected to critically evaluate information, identify trends, and contribute to the development of strategic recommendations. Your work will support decision-making across various business functions, requiring a strong analytical mindset, attention to detail, and a commitment to producing high-quality, evidence-based outputs.

What You’Ll Be Doing:

Extract non-scalable public domain data such as national statistics and trade data and further develop it for use in data estimates.
Manipulate internal Euromonitor data such as price tracking and digital share of shelf to build granularity into data estimates.
Build global and regional company profiles to be used in company and brand data calculations
Work with forecasting specialists to adapt models for regional markets and flag conflicts, validates results against primary research.
Identify relevant sources and critically evaluate information, recognize gaps in research and take logical steps to find the necessary information.
Commission in-country analysts for targeted primary research to fill information gaps and provide local insights. Oversee daily management of ICAs, owning the communication, querying and related admin tasks.
Responsible for data checks throughout data manipulation. Run quality control and provide detailed explanations on sources and data triangulation and the why behind the numbers.
Analyse large datasets and manipulate them as needed to create meaningful category/country estimates, as well as monitoring, reviewing, and cleaning up data for internal and external stakeholders, while maintaining records and resolving quality issues.
Provide explanation and defend our research approach to clients when called upon to do so.
Collaborate with local specialist on basic interaction with clients to build and sustain engagement.
Work closely with other teams providing big data inputs, scalable data sources and local insight.

Requirements

How You’Ll Do It:

Curiosity with a passion for learning, problem-solving, and making a difference combined with flexibility, the ability to embrace diversity and be adaptable to change.
Analytical with strong problem-solving skills, process oriented and quick learner.
Excellent communicator with good listening skills and an openness to new ideas.
Team player with a collaborative and transparent approach, capable of working in a global environment.
Proficiency in English (with other languages an advantage), combined with a high level of numeracy and the confidence to engage trade sources for additional insights.
Strong computer literacy, particularly in MS PowerPoint, Word and Excel, with experience of tools such as Power BI and Tableau.

The advertised gross monthly pay range for this role is: 2,000 - 2,150 Euros / Month.

Benefits

Why work for Euromonitor?

Our Values:

We seek individuals who act with integrity
We look for candidates who are curious about the world
We feel that as a community, we’re stronger together
We seek to enable people to feel empowered
We welcome candidates who bring strength in diversity

International: We have a multinational workforce and communicate daily across our 16 global offices.

Hardworking and Sociable: Our staff balance hard work with enjoyment, offering flexible hours and regular social events, including after-work meetups, summer and Christmas parties.

Committed to Making a Difference: Our Corporate Social Responsibility Programme provides two volunteering days annually; donation amounts for new starters and supports local and international charities through various initiatives.

Excellent Benefits: We offer competitive salaries, healthcare and pensions, generous holiday allowances, hybrid working, and flexible start and finish times.

Opportunities to Grow: We provide extensive training and development, promoting from within and across departments, and rewarding talent.

Equal Employment Opportunity: Euromonitor International does not discriminate based on race, colour, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, genetic information, age, membership in an employee organization, or other non-merit factors.

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Current Employees:

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet.

The Environmental Science and Policy Department at the Rosenstiel School of Marine, Atmospheric and Earth Science at the University of Miami has an exciting full-time position for a Research Associate 1. The employee will work as a researcher in Dr. Katherine Mach’s laboratory.

Duties Include:

Analyzing data on stormwater drainage infrastructure.
Conducting statistical and comparative analyses.
Drafting text summarizing the methods and findings of the research.

Education Requirements (Essential Requirements):

Bachelor's degree in a climate or engineering related discipline is required

Knowledge, Skills, And Abilities:

Excellent critical thinking skills.
Experience with data analysis.
Experience with statistical methods.
Expertise in literature research.
Experience with platforms for data processing and statistical computing, as well as graphics preparation, (e.g., Excel, R, ArcGIS, Adobe Illustrator).

The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.

Job Status:

Part time

Employee Type:

Staff

Pay Grade:

A5","hiringOrganization":{"@type":"Organization","name":"University of Miami","sameAs":"https://www.miami.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"CIMAS Building, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":10,"item":{"@type":"JobPosting","title":"Clinical Research Associate II","datePosted":"2025-09-19","description":"

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

코어팀 Cra 채용 중

*CRA로 허가임상 과제 모니터링 만 1년 이상 경력자 지원 가능*

-> 인터뷰 후 경력 사항에 따라 CRA I - II 혹은 최대 Senior 타이틀 오퍼 예정

CRA 업무 스콥은 Maintenance 부분 참고 부탁드립니다.*
Protocol & ICF amendment 진행 및 In-house work 서포트가 있어 In-house 업무 로드를 덜어드리고 있습니다. (SUSAR reporting, 통관, 연구비 정산 follow up, IRB 문서 다운로드/ 번역 의뢰/ naming 등)*

Key Accountabilities:

Start-up (from site identification through pre-initiation):

Act as Parexel’s direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.

Build relationships with investigators and site staff.
Conduct, drive and manage country specific feasibility and/or site pre-qualification and qualification activities, which may include:
-Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs) and any amendments.
-Conduct remote Qualification Visits (QVs).
Generate visit/contact reports, using judgment to identify site issues and problem solving to direct resolution.
Develop strategy to configure, distribute, and collect, and review and approve, high quality country specific and/or site specific documents or essential regulatory documents (SRP) and any updated or amended regulatory documentation.
Customize, review, and negotiate as needed, country/site specific Informed Consent Forms (ICF), translations (within parameters of country/regulatory/client requirements), and customize and negotiate any amendments.
Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval.
Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy.
Forecast, develop, manage, and revise plans and strategies for:
-IRB/IEC and MoH / RA submission/approval,
-Site activation,
-Patient recruitment & retention.
Update and maintain appropriate Clinical Trial Management systems (CTMS) in a timely manner.
Promptly identify, use judgment and knowledge to address and resolve or escalate, any site question and/or issue, including but not limited to: potential issues or risks with site activation timelines, issues with patient recruitment strategy, deficiencies in training, data quality or integrity, study non-compliance, etc.
Facilitate and support allocated sites with access to relevant study systems and ensure they are compliant with all project specific training requirements prior to study start.
Actively participate in Investigator and other external or internal meetings, audits & regulatory inspections
Work in a self-driven capacity, with limited need for oversight.
Proactively keep manager informed about work progress and any issues.
Maintenance (from initiation through close out):

Act as Parexel’s direct contact with assigned sites, assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve site issues.

Build relationships with investigators and site staff.
Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements.
Evaluate if on-site staff assignment is still accurate and determine and implement corrective actions & follow-up, if necessary / relevant.
Address and resolve issues at sites, including the need for additional training, potential deficiencies in documentation, and communication.
Address/evaluate/resolve issues pending from the previous visit, if any.
Follow-up on and respond to appropriate site related questions.
Apply working knowledge and judgment to identify and evaluate potential data quality and data integrity issues. Determine and implement appropriate follow-up action.
Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required.
Collect, review, and approve (if applicable) updated/amended site documentation, including regulatory documents as applicable.
Evaluate site recruitment plan in collaboration with the site staff on an ongoing basis and provide strategy for improvements.
Perform on-site visits; this includes Qualification and Initiation visits; apply judgment and knowledge to independently resolve site issues, questions and concerns.
Conduct remote visits/contacts as requested/needed.
Generate Visit/Contact Report.
Evaluate overall compliance and performance of sites and site staff: provide recommendations regarding site-specific actions and use judgment and experience to assess the ability and motivation of site staff.
Assess & manage test article/study supply including supply, accountability and destruction/return status.
Review & follow-up site payment status.
Follow-up on CRF data entry, query status, and SAEs.
Conduct on-site study-specific training (if applicable).
Perform site facilities assessments
Recognize impact of study non-compliance/issues/delays/changes on study timelines and communicate study issues that require immediate action, with proposed strategy for resolution

Overall Accountabilities from Site Identification to Close out:

Ensure timely and accurate completion of project goals and update of applicable trial management systems.

Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required.
Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF), ensuring first time quality, and distribute study documents to site including configuration of Investigator Site Files if applicable and on-going maintenance for completeness and quality.
Ensure that assigned sites are audit and inspection ready
Monitor and maintain compliance with ICH-GCP and applicable international and local regulations.
Delegate administrative and other tasks to Administrative Support Team as needed and where appropriate. Guide Administrative Support Team members, review work, and provide feedback to manager regarding performance.
Show commitment and perform consistent high quality work.
Maintain a positive, results-orientated work environment, building partnerships and collaborative relationships, communicating with team(s) in an open, balanced, objective manner, modeling the high performance culture values.
Maintain a working knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, Parexel SOPs, other Parexel / Sponsor training requirements and study specific procedures, plans and training.
Ensure basic understanding of project scope, milestones, budgets, and strive for high quality, timely, and efficient delivery.
Provide input and feedback for Performance Development Conversation(s).
Proactively keep manager informed about work progress and any issues.
Develop expertise to become a subject matter expert.
Work in a self-driven capacity, with limited need for oversight.
Complete additional tasks in a timely manner (e.g. timesheets, expenses, metrics, etc.)

Skills:

Strong problem solving skills
Able to take initiative and work independently, and to proactively seek guidance when necessary.
Excellent Presentation Skills.
Client focused approach to work.
Ability to interact professionally within a client organization.
Flexible attitude with respect to work assignments and new learning.
Ability to prioritize multiple tasks, and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.
Strong ability to make appropriate decisions in ambiguous situations.
Willingness to work in a matrix environment and to value the importance of teamwork.
Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
Excellent interpersonal, verbal, and written communication skills.
Sense of urgency in completing assigned tasks and ability to assist others to meet study/country deliverables.
Excellent time management in order to meet study needs, team objectives, and department goals.
Proven ability to work across cultures.
Shows commitment to and performs consistently high quality work.
Ability to successfully work in a (‘virtual’) team environment.
Consulting Skills.
Able to accommodate travel time requirements, according to tasks allocation/phase of the study assigned.
Act as a mentor and role model for other team members.
Effectively enlist the support of team members in meeting goals.
Attention To Detail.
Holds a driver’s license where required.

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Who We Are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What Clinical Operations Does at Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.

We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us Worldwide!

What you will do

Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits
Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
Actively participate in study team and investigator meetings
Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)

What you will bring to the role

Excellent interpersonal, oral, and written communication skills in English and local language
Superior organizational skills with attention to detail, and the ability to work independently
Broad understanding of clinical research principles and process
Proficiency in Microsoft Office, CTMS, and EDC Systems

Your Experience

At least two years of independent clinical monitoring experience
Demonstrable experience in handling multiple protocols across a range of therapeutic indications
Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree)
Ability to meet the travel requirements of the job

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Must have oncology studies experience as SIT On-site monitoring experienced CRA
Ability to work independently and collaboratively in a fast-paced environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

#Li-Remote

#Li-So1

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Korea, Seoul, Korea, Republic of","addressCountry":"South Korea","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":13,"item":{"@type":"JobPosting","title":"Manager, Population Health Analytics","datePosted":"2025-09-18","description":"Description\n

Position Summary:

Navvis is seeking a highly skilled, experienced, and strategic Manager of Population Health Analytics to join our team. This role is central to identifying and quantifying opportunities to optimize health and healthcare outcomes, risk adjustment, clinical care quality and population health to drive performance improvement across our client base. This role also contributes to projections and evaluations of the financial impacts of new or existing programs and solutions on clinical care delivery, quality and population health. The ideal candidate will bring deep expertise and experience in healthcare quality analytics, clinical performance measurement, and population health strategies—while embodying the core attributes of a high-value analytics professional.

This role operates in a dyad partnership with the Manager of Medical Economics Analytics, ensuring a coordinated approach to identifying clinical and quality performance opportunities alongside cost and utilization insights. Together, these roles form a strategic analytics leadership pair, responsible for delivering integrated, high-impact information to drive action across the organization and to clients.

The Manager of Population Health Analytics will:

Engage regularly with internal and external stakeholders across clinical, operational, and executive teams to align on strategic priorities and analytic needs.
Serve as a trusted advisor, translating complex data into actionable insights that support cost containment and performance improvement.
Collaborate closely with the Manager of Population Health Analyst to ensure consistency, alignment, and synergy across all analytics deliverables and client engagements.
Lead a small team to create a collaborative team environment, providing guidance and support for analysts.

A Day In The Life:

Lead complex analyses focused on illness burden, identification and stratification of populations, clinical quality performance, and risk adjustment.
Identify actionable opportunities to appropriate utilization and optimized cost of care.
Consult and collaborate with clinical, financial, and operational teams internal and external to Navvis to determine and prioritize insights needed, manage delivery, and interpret strategic and tactical implications of insights.
Extract meaningful insights by creating opportunity assessments, driver analyses, dashboards, and other products.
Translate insights into strategic recommendations for internal stakeholders and clients.
Develop and monitor key performance indicators of illness burden, clinical quality, and risk adjustment performance.
Create a culture of continuous improvement and accountability, setting clear expectations and empowering team members to achieve high performance.
Develop, contribute to, and implement best practices and standards that create high-value, meaningful, and accurate insights.
Ensure data and analysis quality, and alignment with enterprise standards.

What Success Looks Like in this Role:

Growth Mindset: Eager to solve problems, learn from challenges, and deliver smarter insights.
Technical Aptitude: Codes efficiently, validates work rigorously, and aligns analysis with role complexity.
Business Fluency: Understands strategic priorities and translates data into high-impact decisions.
Consultative Approach: Delivers tailored insights through agile problem-solving and project management.
Data Storytelling: Crafts and translates compelling narratives with visualizations and presentations.

\nRequirements\n

We are excited about you if you have these things:

Bachelor’s degree in a relevant field—e.g., public health, epidemiology, nursing, allied health, biostatistics, statistics, data science, health services research, healthcare administration, population health, etc.; Master’s degree strongly preferred.
7+ years in healthcare, clinical and/or population health analytics in a payer, health system, or provider organization
1-2 years of people leadership experience is required, 3 years strongly preferred.
Proficiency in SQL and statistical programming (SAS, R, Python, etc.) for data extraction, manipulation, and analysis.
Broad and deep expertise in the use of diverse data sources: claims, clinical, notifications, pharmacy, lab, and social determinants of health; population health metrics, and risk stratification methodologies.
Experience and expertise in value-based care and alternative payment models
Strong communication and project leadership skills, and the ability to share complex information with a variety of audiences.
Expertise with data visualization tools (Tableau, Power BI).
Lead complex analyses focused on clinical performance, quality metrics, and population health outcomes.
Experience with healthcare data platforms, risk scores, quality measurement, and clinical and business rules that segment populations by illness burden, disease states, and other risk factors.

What You'Ll Get:

Navvis is committed to attracting the most insightful and motivated talent by providing a candidate and onboarding experience that you won't find elsewhere! We foster an environment and culture that allow people to be creative, feel connected and be inspired to do their best work no matter where they are on the map. For all colleagues at Navvis, we strive to ensure that they have everything needed to be successful. From the basics like a competitive total rewards strategy, volunteering and social engagement activities to creating company experiences that challenge you to think differently and do different things as part of our never stop learning ecosystem, we support the whole person when you become a team member at Navvis.

Navvis offers a competitive benefits package including, but not limited to, medical, dental, vision, 401K with a safe harbor contribution and Paid Time Off plan starting at 2+ weeks.

Our Commitment:

Navvis is an equal employment opportunity and affirmative action employer seeking diversity in qualified applicants for employment. All applicants will receive consideration for employment without regard to race, ethnicity, color, gender, gender identity, age, religion, creed, national origin, ancestry, disability, perceived disability, medical condition, genetic information, military or veteran status, sexual orientation, or any other protected status, as defined by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodation to complete your application and participate fully in our recruitment experience. Contact us at H.R@navvishealthcare.com.

#Li-Remote

#Mid-Senior

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Eco Process Development Research Associate Ii/Iii

Department: 55 - ECO Process Development
Employment Type: Full Time
Location: Redwood City, CA
Reporting To: Stephan Jenne
Compensation: $74,800 - $121,000 / year

Description

Codexis, a biotechnology company based in Redwood City, CA, is looking to hire a ECO Process Development Research Associate II/III.\n
Codexis is a leading enzyme engineering company leveraging its proprietary CodeEvolver® technology platform to discover, develop and enhance novel, high-performance enzymes and other classes of proteins. Codexis enzymes solve for real-world challenges associated with small molecule pharmaceuticals manufacturing and nucleic acid synthesis. The Company is currently developing its proprietary ECO Synthesis™ platform to enable the scaled manufacture of RNAi therapeutics through an enzymatic route. Codexis enzymes can drive improvements, such as higher yields, reduced energy usage and waste generation, improve efficiency in manufacturing and greater sensitivity in genomic and diagnostic applications.

\nTo meet the goals we’ve set for ourselves, we look for individuals who are driven, eager to grow and ready to embrace meaningful challenges. We empower employees to be authentic, ambitious, agile and have the courage to take action where they can make a positive impact.

\nCome join us on this journey to transform the enzyme engineering landscape for the betterment of human health.

\n
\nAbout the Opportunity The Process Development Research Associate I will join the Process Development group which is part of the TechOps department. Successful candidates will be a part of a dynamic and enthusiastic team responsible for development, scale up and tech transfer of the ECO Synthesis™ platform. The individual will be working with a high performing team with day-to-day laboratory workflows and operations to help with design, optimization, and analysis of ECO Synthesis™ technology. The position is an on-site role located at our Redwood City facility full time.

\nIf any of the below describes you, we would love to meet you!

Possess a passion for being part of the therapeutic community helping bring cutting edge treatments to patients in need.
Enjoys collaboration across different functional groups to get a holistic understanding of process development along with aligning data with internal stakeholders.
Enjoys problem solving by implementing engineering and analytical solutions.

In This Role You Will Be Responsible For:

Assist in the development and optimization of advanced analytical workflows, focusing on High-Performance Liquid Chromatography (HPLC).
Contribute to the development and enhancement of post-synthesis tangential flow filtration methods to ensure product quality.
Follow established protocols and procedures to conduct experiments, maintaining accurate and detailed records.
Collaborate with cross-functional teams to troubleshoot and resolve technical challenges.
Maintain laboratory equipment and ensure compliance with safety and quality standards.\n

The Essential Requirements Of The Job Include:

Bachelor’s degree in Life Sciences or Chemistry with 2+ years of experience, or a Master’s degree.
Basic understanding of laboratory techniques.
Experience with High-Performance Liquid Chromatography (HPLC) is a plus.
Strong attention to detail and ability to follow protocols with supervision.

\n
Additional experience that would be valuable for this role includes:\n

Excellent organizational and communication skills.
Ability to work effectively in a collaborative, team-oriented environment.

CODEXIS PAY TRANSPARENCY: The anticipated salary range for candidates who will work in Redwood City is $36.00 to $45.65/hour for an II and $89,000 to $121,000 for a III. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Codexis is a multi-state employer, and this salary range may not reflect positions that work in other states.

What Can Codexis Offer You?

Medical, Dental and Vision Insurance
Basic Life, AD&D, Short- and Long-Term Disability Insurance
401k with Company Match up to 4%
Company Equity
Generous Paid Time Off including 18 Company Holidays (with a summer and winter shutdown), Vacation, and Wellness Time
Annual Lifestyle Account for reimbursement of fitness programs, equipment and more
Employee Stock Purchase Program (ESPP)
Flexible Spending Accounts (Commuter/Parking, Dependent Care & Healthcare)
Student Debt Program (Company Contribution to Loans)
Mental Health Wellness Program
Subsidized onsite lunch program
Onsite Gym Facilities
Paid Parental Leave
And More!

","hiringOrganization":{"@type":"Organization","name":"Codexis Inc","sameAs":"https://www.codexis.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Redwood City, CA","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":15,"item":{"@type":"JobPosting","title":"Field Research Associate","datePosted":"2025-09-18","description":"

Company Description

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services.
\n
\nTrusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.

SGS is the world’s leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 94,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world.

Job Description

The Field Research Associate will effectively and safely conduct all aspects of field research and development trials under the direction of the location Field Scientist and/or Field Research Manager. The Field Research Associate will safely conduct jobs for which the local management deems they are qualified and adequately trained to complete. Training will be provided on a task-by-task basis.

Specific duties associated with the conduct of field trials and field testing as detailed in SGS SOPs include the following:

Assist local SGS field management personnel in maintaining an up-to-date flow of paperwork
Monitor thermographs and weather data collection
Assist personnel in establishing and maintaining test plots
Conduct plot maintenance and plant protection inputs as required and directed by field management
Assist in field research tasks such as pollinations, sampling, and field data collection
Apply maintenance and test chemicals if hold a pesticide application license under the direction of field
management
Assist in the execution of critical test phases and preparation of the Field Trial Notebooks
Maintain equipment and facilities in accordance with applicable SOPs and in a safe, clean, neat, and
organized manner
Complete assigned duties according to applicable SOPs
Maintain thorough knowledge of GLP requirements, regulatory guidelines, and SGS SOPs

Qualifications

Education And Experience

Associate degree in an agricultural science-based field (preferred)
0-2 years of relevant biological/agricultural field experience (preferred)
Current Pesticide Applicator License (preferred)

Licenses / Certifications

Pesticide Applicator License

Knowledge / Skills / Abilities

Must be able to effectively operate farm equipment, such as tractors, cultivators, and sprayers, and experience with small plot field equipment preferred
Knowledge of and/or experience with GLP requirements is preferred
Must be able to work in a safe manner and foster a safe, sustainable, and environmentally sound field situation
Must be detail-oriented, well organized, and able to
work independently
Excellent communication skills are required
Must be able to work in a fast-paced environment
Knowledge of ARM preferred
Ability to handle a variety of projects effectively,
efficiently, and with confidentiality

Additional Asks

Proficient in Microsoft Office including Word, Excel, and PowerPoint

Physical Demands Of The Job

Stand: Occasional
Move or traverse: Frequent
Sit: Frequent
Use hands: Occasional
Reach with hands and arms: Never
Climb or balance: Never
Stoop, kneel, crouch or crawl: Frequent
Talk/hear: Never
Taste/Smell: Never
Lift/carry/push or pull: Occasional

Environmental And Work Conditions

Wet or humid (non-weather) conditions: Never
Work near moving mechanical parts: Occasional
Work in high, precarious places: Never
Fumes or airborne particles: Never
Toxic or caustic chemicals: Occasional
Outdoor weather conditions: Occasional
Extreme cold (non-weather): Occasional
Extreme heat (non-weather): Occasional
Risk of electrical shock: Never
Work with explosives: Never
Risk of radiation: Never
Vibration: Never
Bio-hazard: Never

Vision Requirement

No Special Vision Requirement
Close Vision (clear vision at 20 inches/50 centimeters or less)
Distance Vision (clear vision at 20 feet/6 meters or more)
Peripheral Vision (ability to observe an area that can be seen up and down or to the left and right while eyes are fixed on a given post)
Depth Perception (three-dimensional vision, ability to judge distance and three-dimensional relationship)
Ability to adjust focus (ability to adjust the eye to bring an object into sharp focus)
Ability to see color

Auditory Requirements

No special auditory requirements
Provide with specific auditory requirements

Health, Safety, And Environment

Fit for Duty Medical Surveillance Requirement – employee must complete a general physical and questionnaire related to physical efforts of job
Accountable for the Health, Safety and Environment performance of self and colleagues and adherence to all regulations as per the Company Health and Safety Manual and the
immediate reporting of any health, safety or environmental incidents, accidents, concerns orhazards to the Manager / Supervisor and H&S representative for action.
Demonstrates good and safe work habits and enforces a clean working environment.
Adheres to all safety management system (OIMS) and quality management system (QMS)
training, policies and procedures, including manuals, test procedures, work instructions and the monitoring and/or verification of equipment and processes relating to testing activities.
Knowledge of good laboratory practices, ex. Health & Safety, working with acids and other
harmful reagents. (only include this line if it is required for the position)

DRUG, ALCOHOL, AND IMPAIRMENT PREVENTION REQUIREMENTS – AS PER OI POLICY

Non-Sensitive - work includes all work not classified as Safety-Sensitive or Risk-Sensitive. Position is subject to post incident and
reasonable cause testing.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Additional Information

SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.

This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company’s rights to assign or reassign duties and responsibilities to this job at any time.

If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.

","hiringOrganization":{"@type":"Organization","name":"SGS","sameAs":"https://sgs.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Wyoming, IL, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":16,"item":{"@type":"JobPosting","title":"Research Associate","datePosted":"2025-09-18","description":"

ECS is seeking a Research Associate to work remotely. Please Note: This position is contingent upon additional funding.

\n\n

ECS is seeking a contractor to provide technical and strategic support with developing and evaluating technology to aid in large whale vessel strike mitigation.

\n\n

Tasks Will Include:

Provide support with coordinating the development and evaluation of technologies for vessel strike mitigation by collaborating with researchers, industry, private sector, USG, and other principal experts as needed.
Support and provide strategic guidance on programs and projects to meet national priorities. Track and assess program effectiveness and provide recommendations for goals and objectives.
Write concise documents such as briefs, memoranda, presentations, and technical correspondence that present scientific and technical information.
Oversee the analysis and interpretation of biological and technical data as well as investigations of new technologies and critical uncertainties, preparation and editing of scientific and technical reports, papers and presentations, and preparation of proposals and projects.
Coordinate with NOAA staff across Headquarters offices, regional offices, and science centers.

Salary Range: $70,000 - $85,000

General Description of Benefits

\nQualifications\n

M.S. in biology, ecology, natural resource management, or other relevant field.
Documented evidence of education and/or experience in one of the following: environmental sciences, biological sciences (fisheries biology/ecology; marine mammal biology/ecology; sea turtle biology/ecology; and/or marine biology/ecology), ecological risk assessment or environmental impact analysis, scientific project management, environmental regulations and the Federal regulatory process.
Strong technical writing and communication skills.
Ability to work effectively both individually and collaboratively in a team/group setting.

","hiringOrganization":{"@type":"Organization","name":"ECS","sameAs":"https://ecstech.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Work from home, VA","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":17,"item":{"@type":"JobPosting","title":"2026 AI Research Associate Program - Internship","datePosted":"2025-09-18","description":"

The goal of J.P. Morgan AI Research is to explore and advance cutting-edge research in AI, including ML as well as related fields like Cryptography, to develop and discover principles of impact to J.P. Morgan’s clients and businesses. JPMorgan Chase AI Research has assembled a team of experts in many fields of AI. They pursue primary research in areas related to our research pillars as well as concrete problems related to financial services. They partner with internal teams to accelerate the adoption of AI within the firm. They also work with leading academic faculty around the world on areas of mutual interest.

As a Research Scientist on the AI Research team, you will conduct end-to-end research typically within a specialized focus area. You will work on multiple research projects in collaboration with internal and external researchers and with applied engineering teams. The team is headquartered in New York and present in London, Madrid, Paris and the Bay Area. Conducting AI research in financial services offers unique and exciting opportunities for impact -- as a member of this highly visible team, you will have the opportunity to realize significant impact not only within J.P. Morgan but also to the broader AI community.

\n\n

Job Responsibilities

You will be integral to all aspects of the research lifecycle such as formulating problems, gathering data, generating hypotheses, developing models and algorithms, conducting experiments, synthesizing results, building prototype applications and communicating the significance of your research.
Your output will result in high-impact business applications, open source software, patents and/or publications in AI/ML conferences and journals. As a member of the AI research community, you will also have the opportunity to participate in relevant top-tier academic conferences to broaden the impact of your contributions.

\n\n

Required qualifications, capabilities, and skills

Currently pursuing a Master’s degree in Computer Science, Statistics, Engineering or related fields.
Extensive programming skills in Python, Java or C++
Proficient understanding of fundamental AI and ML techniques; e.g., A*, regularization
Practical experience with statistical data analysis and experimental design
Demonstrate clear and effective verbal and written communication skills, also has curiosity, creativity, resourcefulness and a collaborative spirit
Demonstrate ability to work on multi-disciplinary teams with diverse backgrounds
Interest in problems related to the financial services domain (specific past experience in the domain is not required)

\n\n

Preferred qualifications, capabilities, and skills

Currently pursuing a PhD in Computer Science (especially AI/ML) or related field.
Research publications in prominent AI/ML venues; e.g., conferences, journals
Strong expertise in one or more specialized areas of relevance to AI in Finance, e.g., LLM-based reasoning, foundational models, AI agents, planning, scheduling and optimization, AI search, multimodal document analytics, AI for coding, knowledge representation, reasoning under uncertainty, task-focused trustworthy AI, cryptography for AI, continuous learning from experience, image and language processing and understanding, large-scale complex data analytics, synthetic data and behavior understanding
Practical experience with ML platforms such as Tensorflow/Keras, PyTorch, etc.
Comfort with rapid prototyping and disciplined software development processes
Practical software engineering experience in collaborative project settings

\n\n\n\n

JPMorganChase, one of the oldest financial institutions, offers innovative financial solutions to millions of consumers, small businesses and many of the world’s most prominent corporate, institutional and government clients under the J.P. Morgan and Chase brands. Our history spans over 200 years and today we are a leader in investment banking, consumer and small business banking, commercial banking, financial transaction processing and asset management.

We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. We also make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as mental health or physical disability needs. Visit our FAQs for more information about requesting an accommodation.

","hiringOrganization":{"@type":"Organization","name":"JPMorgan Chase & Co.","sameAs":"https://www.jpmorganchase.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":18,"item":{"@type":"JobPosting","title":"Staff Research Associate II - Pediatric ADHD Study","datePosted":"2025-09-18","description":"

General Information

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\n\n\n\n\n\nWork Location: Los Angeles, CA, USA\n\n\n\n\n Onsite or Remote\n \n\n Fully On-Site\n \n\n\n\n Work Schedule\n \n\n varied part time shifts during normal business hours: Monday-Friday 8am-5pm\n \n\n\n\n Posted Date\n \n\n 09/17/2025\n \n\n\n\nSalary Range: $28.88 - 46.46 Hourly\n \n\n\n\n Employment Type\n \n\n 4 - Staff: Limited\n \n\n\n\n Duration\n \n\n 11 months\n \n\n\n\n Job #\n \n\n 26807\n \n\n\n\n\n\n\n

Primary Duties And Responsibilities

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The Semel Institute is seeking to hire a part time limited Staff Research Associate II to assist with research support. Duties of the role include but are not limited to the following:

Laboratory Research Support

Conduct assessments with research participants in person, by phone, by video call, and at off
Instruct research participants on the use of behavioral health tracking tools for remote data collection
Administer and score observational measures
Assist with writing protocols, consents, and IRB application and submission materials
Facilitate collection of data, processing of data, and storage of data
Conduct risk assessments in-person or by phone when required, following strict protocols, and promptly sharing risk assessment reports to clinical supervisor
Set-up and maintain testing devices (e.g., sensors, gait analysis, iPads)
Complete subject tracking in database, maintaining project records and project organization
Communicate and coordinate with team members to ensure comprehensive data collection
Participate in study recruitment, team trainings of study staff and volunteers and progress review meetings
Potentially monitor multiple e-mail accounts and voicemail account; respond to inquiries in timely manner
Prepare and maintain study-specific manuals, workflows, training materials
Other duties as needed.

Pay Range: $28.88 - $46.46 hourly.
*Please note that this limited position may convert to career. \n\n\n\n\n\n\n\n

Job Qualifications

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Required:

At least one-year experience in human clinical research studies or in settings with direct relevant patient contact, including training in risk assessment and response protocols
Ability to prioritize and complete in a timely way work on multiple projects with competing requirements
Ability to use multiple online tools to support remote data collection from participants with a range of familiarity with technology
Willingness to complete CareConnect training as needed
Collaborative, able to work both independently and as part of a team
Communicate clearly and effectively both verbally and in writing
Able to work and practice professional relationships with medical personnel, research subjects, patients and families
Strong computer skills including word processing, e-mail systems, file transfer, spreadsheets, matlab software, data entry, database maintenance, including the ability to enter data and maintain study records
Strong time management and interpersonal skills

Preferred:

Bachelor’s Degree in Cognitive Science, Psychology, or related discipline
Previous experience with clinical research in neonatal and pediatric populations
A minimum commitment of two years is preferred
Immediate start date preferred

","hiringOrganization":{"@type":"Organization","name":"UCLA Health","sameAs":"https://www.uclahealth.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Fully On-Site"}}}},{"@type":"ListItem","position":19,"item":{"@type":"JobPosting","title":"Staff Research Associate (Part Time)","datePosted":"2025-09-18","description":"

General Information

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\n Press space or enter keys to toggle section visibility

\n\n\n\n\n\nWork Location: Los Angeles, CA, USA\n\n\n\n\n Onsite or Remote\n \n\n Flexible Hybrid\n \n\n\n\n Work Schedule\n \n\n During the hours of Monday - Friday, 8am - 5pm\n \n\n\n\n Posted Date\n \n\n 09/17/2025\n \n\n\n\nSalary Range: $26.52 - 31.63 Hourly\n \n\n\n\n Employment Type\n \n\n 4 - Staff: Limited\n \n\n\n\n Duration\n \n\n 11 months\n \n\n\n\n Job #\n \n\n 26710\n \n\n\n\n\n\n\n

Primary Duties And Responsibilities

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The Division of Population Behavioral Health at the Semel Institute is seeking a detail-oriented, dedicated, and responsible individual to provide research support and data administration for the 4Youth project. The 4Youth Project is a community partnered participatory research project that aims to improve prevention and early intervention mental health and social services for adolescents and young adults. 4Youth is a multisite research study at UCSF and UCLA, that will co-create with youth a mobile app to support the wellbeing of young people and be used along with peer and family navigators in schools and primary care clinics to improve access to social and emotional supports.

Under the direction of the UCLA PI, you will oversee timely data collection, entry, and database management, track completed work and missing data in an organized process; maintain databases, maintain confidentiality of study participants at all times; and handle other administrative tasks related to the research studies as needed.

Pay Range: $26.52 - $31.63 hourly

\n\n\n\n\n\n\n\n

Job Qualifications

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Bachelor’s degree in science related field, preferred
Working knowledge and experience with MS Word and Excel required. and working knowledge and experience with Dedoose preferred
Demonstrated experience in research, including knowledge of research methods and terminology
Knowledge of social science research, involving patient contact, consent, data collection, and data tracking
Experience in data entry, data checking, data management, and data analysis
Excellent organizational skills with attention to detail
Ability to work independently, sometimes under pressure, and work cooperatively with other staff members
Ability to maintain confidentiality of data and patient information
Excellent interpersonal skills necessary for maintaining the integrity of the study
Ability to work in a timely manner and be flexible with schedules
Ability to problem solve and trouble shoot issues and questions as they arrive

","hiringOrganization":{"@type":"Organization","name":"UCLA Health","sameAs":"https://www.uclahealth.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Flexible Hybrid"}}}},{"@type":"ListItem","position":20,"item":{"@type":"JobPosting","title":"Staff Research Associate","datePosted":"2025-09-18","description":"

General Information

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\n Press space or enter keys to toggle section visibility

\n\n\n\n\n\nWork Location: Los Angeles, CA, USA\n\n\n\n\n Onsite or Remote\n \n\n Flexible Hybrid\n \n\n\n\n Work Schedule\n \n\n Monday - Friday, 8am - 5pm\n \n\n\n\n Posted Date\n \n\n 09/17/2025\n \n\n\n\nSalary Range: $26.52 - 31.63 Hourly\n \n\n\n\n Employment Type\n \n\n 2 - Staff: Career\n \n\n\n\n Duration\n \n\n Indefinite\n \n\n\n\n Job #\n \n\n 26426\n \n\n\n\n\n\n\n

Primary Duties And Responsibilities

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\n Press space or enter keys to toggle section visibility

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Pay Range: $26.52 - $31.63 hourly

\n\n\n\n\n\n\n\n

Job Qualifications

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\n Press space or enter keys to toggle section visibility

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Bachelor’s degree in science related field, preferred
Working knowledge and experience with MS Word and Excel required. and working knowledge and experience with Dedoose preferred
Demonstrated experience in research, including knowledge of research methods and terminology
Knowledge of social science research, involving patient contact, consent, data collection, and data tracking
Experience in data entry, data checking, data management, and data analysis
Excellent organizational skills with attention to detail
Ability to work independently, sometimes under pressure, and work cooperatively with other staff members
Ability to maintain confidentiality of data and patient information
Excellent interpersonal skills necessary for maintaining the integrity of the study
Ability to work in a timely manner and be flexible with schedules
Ability to problem solve and trouble shoot issues and questions as they arrive

","hiringOrganization":{"@type":"Organization","name":"UCLA Health","sameAs":"https://www.uclahealth.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Flexible Hybrid"}}}},{"@type":"ListItem","position":21,"item":{"@type":"JobPosting","title":"Sr. Research Associate, Pediatrics","datePosted":"2025-09-18","description":"Sr. Research Associate, Pediatrics - (879501)

Description

WHY UT SOUTHWESTERN?
With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!

JOB SUMMARY
Works under minimal direction to plan, coordinate, perform, and supervise performance of professional level medical or scientific research assignment related to particular or specialized field of endeavor.

We are seeking a highly skilled research staff personnel member with expertise in murine models of liver disease, including neonatal handling, injection techniques, and tissue harvest. The ideal candidate will have experience in epithelial organoid culture from human liver tissues, immunofluorescence imaging, and co-culture assays to study epithelial-immune interactions, as well as familiarity with IACUC/IRB compliance and transcriptomic data interpretation.

Other Desired Experience Includes:

Proficiency in neonatal and adult mouse handling, injections (e.g., intraperitoneal, retro-orbital), and tissue harvest.
Experience with murine models of biliary atresia, including rotavirus infection protocols, monitoring survival, and scoring disease severity.
Immunofluorescence and confocal microscopy for liver and bile duct tissues.
Expertise in isolating and expanding epithelial organoids from human liver and bile duct biopsies.
Skilled in 3D culture systems using basement membrane extracts (e.g., Matrigel, BME), and media optimization.
Handling of organoids derived at both diagnosis and post-transplantation from pediatric patients.
Proliferation, viability, apoptosis, and differentiation assays.
Co-culture assays with immune cells to assess epithelial-immune interactions.
Familiarity with transcriptomic data interpretation (e.g., from RNA-seq, scRNA-seq) is a plus.
Understanding of animal welfare regulations and human biospecimen research policies
Experience in preparing and updating IACUC and IRB protocols.

BENEFITS
UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:

PPO medical plan, available day one at no cost for full-time employee-only coverage
100% coverage for preventive healthcare-no copay
Paid Time Off, available day one
Retirement Programs through the Teacher Retirement System of Texas (TRS)
Paid Parental Leave Benefit
Wellness programs
Tuition Reimbursement
Public Service Loan Forgiveness (PSLF) Qualified Employer
Learn more about these and other UTSW employee benefits!

Experience And Educationrequired

EducationPhD with major coursework in field of assignment and no experience or Master's Degree with major coursework in field of assignment or Bachelor's Degree with major coursework in field of assignment or
ExperienceNo experience required with PhD or 5 years of laboratory experience with a Master's Degree including at least 2 years at level of Research Associate or equivalent or 6 years of laboratory experience with a Bachelor's Degree including at least 2 years at level of Research Associate or equivalent

Job Duties

Organizes laboratory to which assigned; determines work assignments of subordinates, advising them as to techniques, procedures, and equipment to be utilized in solution of work problems; reviews completed work for professional quality and attainment of desired results.
Compiles and evaluates research data, and develops new or revised techniques and procedures based upon such data.
Performs or supervises design, development, or adaptation of equipment or apparatus used in experiments or research to obtain desired results.
Compiles and analyzes results of research assignments and submits to principal investigator.
Instructs medical students, graduate students, residents, and other laboratory personnel of lower grade with respect to techniques, procedures, and equipment utilized in research or experiments.
Confers with industrial, governmental, or other professional groups with respect to progress or results of research assignment.
Assists principal investigator and other professional personnel in preparation of reports and papers for publication, usually exercising responsibility for writing of particular segment or phase of report or paper.
Performs other duties as assigned.

SECURITY AND EEO STATEMENT
Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information. To the extent this position requires the holder to research, work on, or have access to critical infrastructure as defined in Section 113.001(2) of the Texas Business and Commerce Code, the ability to maintain the security or integrity of the critical infrastructure is a minimum qualification to be hired and to continue to be employed in the position.

EEO Statement
UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.

Primary Location

: Texas-Dallas-5323 Harry Hines Blvd

Work Locations

: 5323 Harry Hines Blvd 5323 Harry Hines Blvd Dallas 75390

Job

: Research & Laboratory

Organization

: 423008 - PD-Gastroenterology

Schedule

: Full-time

Shift

: Day Job

Employee Status

: Regular

Job Type

: Standard

Job Posting

: Sep 18, 2025, 11:44:38 AM","hiringOrganization":{"@type":"Organization","name":"UT Southwestern Medical Center","sameAs":"https://www.utsouthwestern.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Texas-Dallas-5323 Harry Hines Blvd","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":22,"item":{"@type":"JobPosting","title":"Research Associate 2","datePosted":"2025-09-18","description":"

Company Description

Syngenta Seeds is one of the world’s largest developers and producers of seed for farmers, commercial growers, retailers and small seed companies. Syngenta seeds improve the quality and yields of crops. High-quality seeds ensure better and more productive crops, which is why farmers invest in them. Advanced seeds help mitigate risks such as disease and drought and allow farmers to grow food using less land, less water and fewer inputs.

Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions.

Syngenta Seeds is headquartered in the United States

Job Description

We are hiring a Research Associate 2 to lead the execution of corn and soybean nursery seed production, strictly follow HSE and Stewardship practices, provide quality seed meeting quantity and timeline targets to assist scientists in delivering project goals, as well as to support site management with the functional activities of a research station.

Accountabilities:

Functioning as an integral member of a team leading aspects of packaging, planting, cultivating, note taking, processing and harvesting in seed production nurseries.
Responsible for efforts to maintain integrity of seed inventory, packaging, field layout, pollinating, seed processing, and data collection.
Performing all tasks and behaving in a manner compliant with and in support of all safety and stewardship related company policies and practices, including completing all required company training courses.
Assist in the automatic seed packaging facility in Nevada, Iowa during peak seasons.
Operate and troubleshoot specialized seed research equipment, including harvesters, seed processing, and packaging equipment.
Provide daily direction to contract staff and task specific training to FTEs and contract staff.
Leading complex projects and deliver on key target, including understanding and operating within given budget.

Qualifications

Associate’s degree in Agriculture, Operations Management, or related field; or 2+ years of relevant experience.
Experience with precision agriculture equipment and software systems.
A basic understanding of plant genetics and breeding is desirable.
Clear understanding of the practices and procedures that affect nursery seed production quality, quantity, and timelines.
Demonstrated outstanding communication skills and experience working with interdisciplinary teams.
A valid driver’s license with an acceptable driver’s history.
Ability to obtain a chemical applicator's license within 3-6 months of hire date is strongly recommended.
Capable of working in high or low temperature conditions in field.
Capable of lifting up to 50 pounds.
Capable of working long hours during time-critical periods of the growing season.

Additional Information

What We Offer:

A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs.
Full Benefit Package (Medical, Dental & Vision) that starts your first day.
401k plan with company match, Profit Sharing & Retirement Savings Contribution.
Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits.

Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: https://www.youtube.com/watch?v=OVCN_51GbNI

Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

WL: 2A

#Li-Onsite #Li-Do1

","hiringOrganization":{"@type":"Organization","name":"Syngenta Group","sameAs":"https://www.syngenta.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Nevada, IA, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":23,"item":{"@type":"JobPosting","title":"Research Associate 2","datePosted":"2025-09-18","description":"

Company Description

Syngenta Seeds brings farmers more vigorous, stronger, resistant plants, including innovative hybrid varieties and biotech crops that can thrive even in challenging growing conditions.

Syngenta Seeds is headquartered in the United States

Job Description

Accountabilities:

Functioning as an integral member of a team leading aspects of packaging, planting, cultivating, note taking, processing and harvesting in seed production nurseries.
Responsible for efforts to maintain integrity of seed inventory, packaging, field layout, pollinating, seed processing, and data collection.
Performing all tasks and behaving in a manner compliant with and in support of all safety and stewardship related company policies and practices, including completing all required company training courses.
Assist in the automatic seed packaging facility in Nevada, Iowa during peak seasons.
Operate and troubleshoot specialized seed research equipment, including harvesters, seed processing, and packaging equipment.
Provide daily direction to contract staff and task specific training to FTEs and contract staff.
Leading complex projects and deliver on key target, including understanding and operating within given budget.

Qualifications

Associate’s degree in Agriculture, Operations Management, or related field; or 2+ years of relevant experience.
Experience with precision agriculture equipment and software systems.
A basic understanding of plant genetics and breeding is desirable.
Clear understanding of the practices and procedures that affect nursery seed production quality, quantity, and timelines.
Demonstrated outstanding communication skills and experience working with interdisciplinary teams.
A valid driver’s license with an acceptable driver’s history.
Ability to obtain a chemical applicator's license within 3-6 months of hire date is strongly recommended.
Capable of working in high or low temperature conditions in field.
Capable of lifting up to 50 pounds.
Capable of working long hours during time-critical periods of the growing season.

Additional Information

What We Offer:

A culture that celebrates diversity & inclusion, promotes professional development, and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs.
Full Benefit Package (Medical, Dental & Vision) that starts your first day.
401k plan with company match, Profit Sharing & Retirement Savings Contribution.
Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits.

Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: https://www.youtube.com/watch?v=OVCN_51GbNI

WL: 2A

#Li-Onsite #Li-Do1

","hiringOrganization":{"@type":"Organization","name":"Syngenta Group","sameAs":"https://www.syngenta.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Slater, Iowa, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":24,"item":{"@type":"JobPosting","title":"Clinical Research Associate II","datePosted":"2025-09-18","description":"

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

PSI’s business is about conducting clinical research of novel medications. We work at the interface of R&D, pharmaceutical industry and healthcare science and provide services to big and mid-sized pharmaceutical companies. We help our clients to generate data about safety and efficacy of medications and bring the best ones to market. By conducting global clinical research trials, PSI makes cutting-edge treatment available in drugstores all over the world and helps patients with serious medical conditions to improve or even save their life. Help us to make sure that PSI medical and business documents are clear to patients, physicians, regulatory authorities, and clients.

We offer an inspiring story of the company that has grown organically from a handful of countries to global presence. PSI is a mature company with standards and practices, but we do not stand still. Every day, there is a figurative Everest to climb, and you will not get bored here.

Job Description

We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in South Korea, Seoul. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Hybrid in Seoul, South Korea

You Will:

Conduct and report all types of onsite monitoring visits
Be involved in study startup
Perform CRF review, source document verification and query resolution
Facilitate site budgets and contract negotiations
Monitor trial progress on the country level
Be responsible for site communication and management
Be a point of contact for in-house support services and vendors
Communicate with internal project teams regarding study progress
Participate in feasibility research
Support regulatory team in preparing documents for study submissions

Qualifications

College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
Independent on-site monitoring experience in Korea
Experience in all types of monitoring visits in Phase II and/or III
Experience in feasibility assessment and study set-up process is preferable
Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus
Full working proficiency in English and Korean
PC skills to be able to work with MS Word, Excel and PowerPoint
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

","hiringOrganization":{"@type":"Organization","name":"PSI CRO","sameAs":"https://www.psi-cro.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Seoul, Seoul, Korea, republic of","addressCountry":"South Korea","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":25,"item":{"@type":"JobPosting","title":"Asset Management - Credit Research Associate - Shanghai","datePosted":"2025-09-18","description":"

Job Summary:

As an Analyst in Fixed Income Research, you will help to conduct and facilitate industry analysis and company-specific coverage. This involves core research ranging from dissecting earnings releases and regulatory filings to assessing relevant news events, macro trends, modelling financial statements and industry dynamics, performing detailed valuation work, writing research notes and sector pieces and making investment recommendations.

\n\n

Job Responsibilities:

Follow specific sectors and companies in China onshore credit market
Provide timely analysis and recommendation on covered companies and sectors
Formulate sector strategies and investment recommendations
Effectively communicate thoughts, ideas and analysis in written and oral form
Maintaining regular contact with GFICC colleagues globally , taking part in conference calls and responding to project requests

\n\n

Required Qualifications, Capabilities, And Skills:

Past experience in China onshore credit research/investment role
Demonstrate a strong ability to address risk and be comfortable with risk-taking
Strong written and oral communication skills
Strong financial analytical skills
Ability to work effectively with colleagues based in around the world

\n\n

Preferred Qualifications, Capabilities, And Skills:

Proficiency in English

\n\nJ.P. Morgan is a global leader in financial services, providing strategic advice and products to the world’s most prominent corporations, governments, wealthy individuals and institutional investors. Our first-class business in a first-class way approach to serving clients drives everything we do. We strive to build trusted, long-term partnerships to help our clients achieve their business objectives.
\n\n \n \n We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. We are an equal opportunity employer and place a high value on diversity and inclusion at our company. We do not discriminate on the basis of any protected attribute, including race, religion, color, national origin, gender, sexual orientation, gender identity, gender expression, age, marital or veteran status, pregnancy or disability, or any other basis protected under applicable law. We also make reasonable accommodations for applicants’ and employees’ religious practices and beliefs, as well as mental health or physical disability needs. Visit our FAQs for more information about requesting an accommodation.","hiringOrganization":{"@type":"Organization","name":"JPMorgan Chase & Co.","sameAs":"https://www.jpmorganchase.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Shanghai, China","addressCountry":"China","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":26,"item":{"@type":"JobPosting","title":"Clinical Research Associate - Sponsor Dedicated","datePosted":"2025-09-18","description":"

Job Overview:
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions:
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications:
• Bachelor's Degree Degree in scientific discipline or health care preferred. Req
• Requires at least 1.5 years of year of on-site monitoring experience. Req
• Equivalent combination of education, training and experience may be accepted in lieu of degree. Req
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $57,500.00 - $226,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.","hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://www.iqvia.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Durham, North Carolina, United States of America","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":27,"item":{"@type":"JobPosting","title":"Senior Clinical Research Associate (NY/NJ)","datePosted":"2025-09-18","description":"Sr. Clinical Research Associate NY/NJ

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Must be located in NY/NJ area
Oncology monitoring experience required
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":28,"item":{"@type":"JobPosting","title":"Clinical Research Associate 2 - IQVIA Biotech","datePosted":"2025-09-18","description":"

IQVIA Biotech is hiring Clinical Research Associate in Spain!

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.

The ideal candidate will have varied therapeutic experience and be willing to working across multiple therapeutics including: Oncology, Hematology, Cardiovascular, etc. This role will be home-based in Spain.

Essential Functions

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

Bachelor's Degree in scientific discipline or health care preferred
Requires at least 1.5 years of on-site monitoring experience
Equivalent combination of education, training and experience may be accepted
Organizational, time management and problem-solving skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Flexibility To Travel
Driver’S License

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.

","hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://www.iqvia.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Madrid, Spain","addressCountry":"Spain","addressRegion":"Europe"}}}},{"@type":"ListItem","position":29,"item":{"@type":"JobPosting","title":"Sr. Clinical Research Associate- Mid-West","datePosted":"2025-09-18","description":"Senior Clinical Research Associate

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":30,"item":{"@type":"JobPosting","title":"Sr. Clinical Research Associate- Northeast","datePosted":"2025-09-18","description":"Senior Clinical Research Associate

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":31,"item":{"@type":"JobPosting","title":"Research Associate","datePosted":"2025-09-18","description":"

Job Description:

• Analysis of routine samples (product development batches, stability study samples, raw materials etc.).
• Operation and Calibration of analytical instruments/equipment’s.
• Analytical activities related to Quality control department.
• Qualification of working standards.
• Documentation of analytical activities as per good documentation practices.
• Work in laboratory as per good laboratory practices.
• To use PPEs and follow safe practices in lab.
• Any other task assigned by management.
• Sampling of raw materials from pilot plant dispensing area.
• Analysis of samples in quality control laboratory.
• Operation and Calibration of instruments in quality control laboratory

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

Job Family:

Product Development

Division:

EPD Established Pharma

Location:

India > Mumbai : Mumbai Development Center - EPD

Additional Locations:

Work Shift:

Standard

Travel:

Not specified

Medical Surveillance:

Not Applicable

Significant Work Activities:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)","hiringOrganization":{"@type":"Organization","name":"Abbott","sameAs":"https://www.abbott.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"India - Mumbai : Mumbai Development Center - EPD","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":32,"item":{"@type":"JobPosting","title":"Clinical Research Associate (CRA) II/ Senior CRA | Melbourne, Sydney, Brisbane","datePosted":"2025-09-18","description":"

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Summarized Purpose:

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or supervising environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix.

Location Information

This is a home-based position and preferably based in Melbourne, Sydney or Brisbane.

Key Responsibilities

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts supervising tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable.
Participates in investigator meetings as vital. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
Ensures that required crucial documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
Contributes to other project work and initiatives for process improvement, as required.

Keys To Success

Education And Experience:

Bachelor's degree in a life sciences related fielder a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship. Valid driver's license where applicable.
Therapeutic experience in Oncology essential
Phase I experience essential

Knowledge, Skills And Abilities:

Proven clinical monitoring skills.
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a solid understanding of ICH GCPs, applicable regulations and procedural documents.
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes.
Good oral and written communication skills, with the ability to communicate effectively with medical personnel.
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues.
Good organizational and time management skills
Effective interpersonal skills.
Attention to detail.
Ability to remain flexible and adaptable in a wide range of scenarios.
Ability to work in a team or independently as required.
Good digital literacy: solid knowledge of Microsoft Office and the ability to learn appropriate software.
Good English language and grammar skills.
Good presentation skills.
Australian citizenship or permanent residency required

Benefits

Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer.

Health & Wellbeing: Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues.
Flexibility: Balance your work and personal life with flexible arrangements.
Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.
Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you.
Learning & Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.

Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender Equality

We offer competitive remuneration, annual incentive plan bonus, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

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We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, (min. 2 years of independent monitoring experience) with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

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What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":35,"item":{"@type":"JobPosting","title":"Senior Clinical Research Associate (Nashville or Atlanta area)","datePosted":"2025-09-18","description":"Sr. Clinical Research Associate

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Must be located in Nashville or Atlanta area
Oncology monitoring experience required
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":36,"item":{"@type":"JobPosting","title":"Experienced Clinical Research Associate - Multi-Sponsored Model","datePosted":"2025-09-18","description":"If you want to do your next step as a CRA, this is your chance!

You’ll have training and development to plan and progress your career in the direction you choose. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

While Projects Vary, Your Typical Responsibilities Might Include

Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication plus administering protocol and related study training to assigned sites
Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

You Should Have

A Bachelor's degree in a health care or other scientific discipline or educational equivalent
At least 1,5 - 2 years of on-site monitoring experience
Fluent in Arabic and English language
Good written and verbal communication skills including good command of English language
Requires frequent travel to sites
Flexible about location, but location must have good connectivity to travel
Homebased
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.
Connect to great opportunity™

","hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://www.iqvia.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Riyadh, Saudi Arabia","addressCountry":"Saudi Arabia","addressRegion":"Middle East"}}}},{"@type":"ListItem","position":37,"item":{"@type":"JobPosting","title":"Sr Clinical Research Associate (NC or FL)","datePosted":"2025-09-18","description":"Sr. Clinical Research Associate NC or FL

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Must be located in NC or FL area
Oncology monitoring experience required
Fluency in Spanish is nice to have
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":38,"item":{"@type":"JobPosting","title":"Clinical Research Associate 2","datePosted":"2025-09-18","description":"

Are you passionate about science, driven by purpose, and ready to make a real impact in the world of clinical research? We’re looking for a Clinical Research Associate 2 who’s ready to take their career to the next level—working on cutting-edge studies that shape the future of medicine. Ideally Sydney or Melbourne. This role is on our Single Sponsor team

Please note as part of the assessment you will be asked to complete a short video screening interview.

Essential Functions:

Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained.
Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success.
Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.

What You Bring

A degree in life sciences or healthcare (or equivalent experience).
18 months minimum on-site Independant monitoring experience to be considered, ideally haemotology.
Deep knowledge of GCP, ICH, and clinical trial operations.
Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad).
A proactive mindset, strong communication skills, and a passion for excellence.

Why Join Us?

Work on diverse, global studies across multiple therapeutic areas.
Be part of a supportive, innovative team that values your growth.
Enjoy flexible work arrangements, travel opportunities, and career develop

","hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://www.iqvia.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"North Sydney, New South Wales, Australia","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":39,"item":{"@type":"JobPosting","title":"Sr. Clinical Research Associate- CST","datePosted":"2025-09-18","description":"Senior Clinical Research Associate

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":40,"item":{"@type":"JobPosting","title":"Research Associate (m/f/d)","datePosted":"2025-09-18","description":"\n\n\nKarriere\n\n\n\n\n\n\n

Research Associate (M/F/D)

\n\nZahnerhaltung\n38.5 Stunden\nauf 24 Monate befristet\nab 01.11.2025\n\n\nEingruppierung gemäß TV-L\nBewerbungsfrist 30.10.2025\n\n\n\n\n

Universitätsklinikum Erlangen
Dental Clinic 1, Research Laboratory for Dental Biomaterials
Prof. Dr. Ulrich Lohbauer
Glückstr. 11
91054 Erlangen

Ansprechperson Bei Fragen:

Prof. Dr. Ulrich Lohbauer
Tel. 09131 85-43740

\n\n\n

VeröFfentlicht Seit:

Job-Nr.: 11318

\nHinweise für Bewerbende\n
\nJetzt bewerben\n\n\n\n\n\n\n

Klingt Spannend? Das Sind Wir:

In the Dental Clinic 1 of the University Hospital Erlangen, the preservation of the patient's own teeth is at the forefront of the treatment spectrum. The Research Laboratory for Dental Biomaterials, as part of Dental Clinic 1, works on scientific research projects and supports dental teaching on current issues. Find out more about the Research Laboratory for Dental Biomaterials at Dental Clinic 1.

\n\n

Your Tasks:

\n\n As part of your DFG-funded work, you will develop and research innovative ways to improve the mechanical resistance of dental glass-ceramics. Your field of work ranges from the glass melting process to the modification of the microstructure with regard to reinforcement concepts and the characterization of newly developed glass-ceramic materials. You will work closely with other team members and project partners to ensure efficient project processing. The project offers you the opportunity to use scientific methods flexibly to meet complex challenges while pursuing a clearly defined overall goal.
\n\n\n\n

Know-How:

\n\n

Completed studies in engineering, ideally in the fields of materials science, materials engineering, dental technology, or comparable training
High level of self-motivation with a willingness to learn and acquire new skills
sound knowledge in the fields of inorganic materials (glass and ceramics) and fracture mechanics
strong organizational and communication skills with the ability to work effectively in an international team
Independent, creative, goal-oriented and solution-oriented working style
very good written and spoken communication skills in German and English
Willingness to travel domestically and abroad is required

\n\n\n\n\n\n\n\n\n\n\n\n\n

We Offer:

\n\n

A classification in the E 13 TV-L pay group
A challenging, varied and responsible position in an exciting field of research
A pleasant working atmosphere, flexible working hours and flat hierarchies
Comprehensive induction training and a wide range of further and advanced training opportunities for personal and professional qualification
Family-friendly environment at Erlangen University Hospital
Support in the search for childcare places or emergency care for relatives in need of care

\n\nAlle Benefits am UKER\n\n\n\n

Teilen ErwüNscht

\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n","hiringOrganization":{"@type":"Organization","name":"Universitätsklinikum Erlangen","sameAs":"https://www.uk-erlangen.de/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Extern & BA"}}}},{"@type":"ListItem","position":41,"item":{"@type":"JobPosting","title":"Sr Clinical Research Associate (Western Canada)","datePosted":"2025-09-18","description":"Sr. Clinical Research Associate (Western Canada)

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Must be located in Western Canada area
Oncology monitoring experience required
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":42,"item":{"@type":"JobPosting","title":"Sr Clinical Research Associate (NJ/NY)","datePosted":"2025-09-18","description":"Sr. Clinical Research Associate - NY/NJ

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Oncology Experience Required
Must be located in NY/NJ area
Ability to travel at least 60% of the time and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":43,"item":{"@type":"JobPosting","title":"Sr. Clinical Research Associate","datePosted":"2025-09-18","description":"Senior Clinical Research Associate

What You Will Be Doing:

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

Advanced degree in a relevant field such as life sciences, nursing, or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What Icon Can Offer You:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life Assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

","hiringOrganization":{"@type":"Organization","name":"ICON plc","sameAs":"https://www.iconplc.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"US, Blue Bell (ICON), United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":44,"item":{"@type":"JobPosting","title":"Research Associate II - Fermentation","datePosted":"2025-09-17","description":"

About Pivot Bio:

Fueled by an innovative drive and a deep understanding of microbiology, genomics, crop nutrition and agriculture, Pivot Bio is pioneering game-changing advances in fertilizer technology. Our first commercial product harnesses the power of naturally-occurring microbes, modern gene editing and application technologies to provide nitrogen to crops. We are dedicated to providing new solutions for farmers to improve yield as they work to help feed the world’s growing population. Read/Hear more about Pivot Bio on Forbes or PBS News Hour.

We are looking for a Research Associate II who thrives in fast-paced industry research lab environment and is motivated by Pivot Bio’s mission to provide microbial-based solutions for nitrogen delivery to crops. The successful candidate should be willing to learn and support innovation, while maintaining excellent laboratory practices.

Reporting to the Scientist, Fermentation, the candidate will be responsible for supporting the development of microbial fermentation processes intended to increase product quality and shelf-life, and improve nitrogen-use efficiency in selected crops. An ideal candidate has passion and solid working knowledge of fermentation processes and operating equipment, including high-throughput, multi-parallel (e.g., Sartorius ambr250), and/or bench-scale fermentation systems. Familiarity with centrifugation and/or tangential flow filtration (TFF) systems, laboratory automation, and LIMS systems are a plus. The candidate should have a working knowledge of microbiology and chemistry, an eye for detail, excellent communication skills, and the ability to thrive in a fast-paced environment with changing research objectives.

\n\n

Key Responsibilities:

Working in a fermentation and downstream laboratory setting with minimal supervision
Operate and maintain lab-scale fermentation systems
Prepare end of fermentation samples for live cells separation and drying
Plate and count microbes using aseptic technique, automated dilution and counting methods
Collect, enter, and analyze fermentation data in LIMS systems
Attend and present data in R&D meetings

\n\n\n\n\n\n\n

Required Education & Experience 

Bachelor of Science degree in life sciences, food science, biological systems engineering, biochemical engineering, or related field or equivalent experience    
Minimum of 2 years of experience in a fast-paced industry fermentation lab environment   
Excellent communication skills and ability to work independently, ask good questions, and recognize anomalies 
Can-do attitude, strong problem solving and troubleshooting skills
Open mind for learning and contributing across fermentation and downstream process development

\n\n\n\n\n\n

Must Be Authorized to Work in the United States

\n\n

What We Offer:

Competitive package in a disruptive startup
Stock options
Health/Dental/Vision insurance with employer-paid premiums
Life, Short-Term and Long-Term Disability policies
Employee Assistance Program with free referrals and discounts
401(k) plan, 3% Match
Commuter benefits
Annual Training & Development support
Flexible vacation policy with a generous holiday schedule
Exciting opportunity to work with a talented and fun team

\n\n

#Li-Onsite

All remote positions and those not located in our Berkeley facility are paid based on National Benchmark data. Following employment, growth beyond the hiring range is possible based on performance.

Hiring Compensation Range$64,000—$80,000 USD","hiringOrganization":{"@type":"Organization","name":"Pivot Bio","sameAs":"https://www.pivotbio.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"St. Louis, MO","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":45,"item":{"@type":"JobPosting","title":"Research Associate II - Downstream","datePosted":"2025-09-17","description":"

About Pivot Bio:

We are looking for a Research Associate II who thrives in a fast-paced industry research lab environment and is motivated by Pivot Bio’s mission to provide microbial-based solutions for nitrogen delivery to crops. The successful candidate should be willing to learn and support innovation, while maintaining excellent laboratory practices.

Reporting to the formulation scientist, downstream, the candidate will be responsible for supporting the downstream processes development intended to increase product quality and shelf-life, and improve nitrogen-use efficiency in selected crops. Prior experience with drying technologies including freeze drying and spray drying is a plus. The candidate should have a strong foundation in chemistry, a working knowledge of microbiology, an eye for detail, skill with troubleshooting laboratory equipment, and excellent verbal and written communication skills. Familiarity with fermentation systems, laboratory automation, and LIMS systems are a plus.

\n\n

Key Responsibilities:

Working in a fermentation and downstream laboratory setting with minimal supervision
Handling end of fermentation samples for live cells separation and drying
Operate and maintain lab-scale processing equipment, including cell separation, freeze-dryer and spray-dryer systems
Plate and count microbes using aseptic technique, automated dilution and counting methods
Collect, enter, and analyze downstream data in LIMS systems
Attend and present data in R&D meetings

\n\n\n\n\n\n\n

Required Education & Experience 

Bachelor of Science degree in life sciences, food science, biological systems engineering, biochemical engineering, or related field or equivalent experience    
Minimum of 2 years of experience in a fast-paced industry fermentation and downstream lab environment   
Excellent communication skills and ability to work independently, ask good questions, and recognize anomalies 
Attention to detail, skilled in making observations and documenting anomalies 
Can-do attitude, strong problem solving and troubleshooting skills
Open mind for learning and contributing across fermentation and downstream process development

\n\n\n\n\n\n\n

Must Be Authorized to Work in the United States

\n\n

What We Offer:

Competitive package in a disruptive startup
Stock options
Health/Dental/Vision insurance with employer-paid premiums
Life, Short-Term and Long-Term Disability policies
Employee Assistance Program with free referrals and discounts
401(k) plan, 3% Match
Commuter benefits
Annual Training & Development support
Flexible vacation policy with a generous holiday schedule
Exciting opportunity to work with a talented and fun team

\n\n

#Li-Onsite

All remote positions and those not located in our Berkeley facility are paid based on National Benchmark data. Following employment, growth beyond the hiring range is possible based on performance.

Hiring Compensation Range$64,000—$80,000 USD","hiringOrganization":{"@type":"Organization","name":"Pivot Bio","sameAs":"https://www.pivotbio.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"St. Louis, MO","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":46,"item":{"@type":"JobPosting","title":"Research Associate - Department of Immunology and Immunotherapy - 106333 - Grade 6","datePosted":"2025-09-17","description":"

Position Details

Department of Immunology and Immunotherapy, School of Infection, Inflammation and Immunology, College of Medicine and Health

Location: University of Birmingham, Edgbaston, Birmingham UK

Full time starting salary is normally in the range £33,002 to £35,608 with potential progression once in post to £39,906

Grade: 6
Part Time (22.5 hours per week)
Fixed Term contract up to June 2027
Closing date: 9th October 2025

Background

To assist in research (by carrying out data collection or analyses) to create knowledge through providing research support for projects and research groups.

The research focus for the group involves studying immune deficiency in blood cancer patients.

Role Summary

Enthusiastic and motivated person to work in the research group of Dr Helen Parry based in Immunology and Immunotherapy at UoB. The research focus for the group involves studying immune deficiency in blood cancer patients.
Work within the blood cancer immunity research group of Dr Helen Parry.
Operate within area of specialism.
Contribute to publications.

Main Duties

Collect research data; input data from visits to local NHS sites.
Process and analyse research data as directed adhering to GCP and GDPR.
Present research outputs, including contributing to academic publications or parts thereof, for example at seminars and as posters.
Develop database and liaise with UoB Redcap team.
Provide guidance as required to support staff and any students who may be assisting with research.
Carry out administrative tasks related directly to the delivery of the research including ethics approval.
Promotes equality and values diversity acting as a role model and fostering an inclusive working culture

Person Specification

GCP trained.
Experience of working within healthcare desirable.
Degree or equivalent in a relevant subject area.
Practical experience of applying the relevant skills and techniques.
Ability to analyse information and communicate effectively.
Ability to access and organise resources successfully.
Knowledge of the protected characteristics of the Equality Act 2010, and how to actively ensure in day to day activity in own area that those with protected characteristics are treated equally and fairly.

Further particulars can be found here

Informal enquiries to Lisa Powell, email: l.h.powell@bham.ac.uk

We believe there is no such thing as a 'typical' member of University of Birmingham staff and that diversity in its many forms is a strength that underpins the exchange of ideas, innovation and debate at the heart of University life. We are committed to proactively addressing the barriers experienced by some groups in our community and are proud to hold Athena SWAN, Race Equality Charter and Disability Confident accreditations. We have an Equality Diversity and Inclusion Centre that focuses on continuously improving the University as a fair and inclusive place to work where everyone has the opportunity to succeed. We are also committed to sustainability, which is a key part of our strategy. You can find out more about our work to create a fairer university for everyone on our website.

","hiringOrganization":{"@type":"Organization","name":"University of Birmingham","sameAs":"https://www.birmingham.ac.uk/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":47,"item":{"@type":"JobPosting","title":"Senior Research Associate, Genomics Platform","datePosted":"2025-09-17","description":"

About Arc Institute

The Arc Institute is a new scientific institution conducting curiosity-driven basic science and technology development to understand and treat complex human diseases. Headquartered in Palo Alto, California, Arc is an independent research organization founded on the belief that many important research programs will be enabled by new institutional models. Arc operates in partnership with Stanford University, UCSF, and UC Berkeley.

While the prevailing university research model has yielded many tremendous successes, we believe in the importance of institutional experimentation as a way to make progress. These include:

Funding: Arc fully funds Core Investigators’ (PIs’) research groups, liberating scientists from the typical constraints of project-based external grants.
Technology: Biomedical research has become increasingly dependent on complex tooling. Arc Technology Centers develop, optimize, and deploy rapidly advancing experimental and computational technologies in collaboration with Core Investigators.
Support: Arc aims to provide first-class support—operationally, financially, and scientifically—that will enable scientists to pursue long-term high risk, high reward research that can meaningfully advance progress in disease cures, including neurodegeneration, cancer, and immune dysfunction.
Culture: We believe that culture matters enormously in science and that excellence is difficult to sustain. We aim to create a culture that is focused on scientific curiosity, a deep commitment to truth, broad ambition, and selfless collaboration.

Arc has scaled to nearly 200 people. With $650M+ in committed funding and a state of the art new lab facility in Palo Alto, Arc will continue to grow quickly in the coming years.

About The Position

We are looking for a highly skilled, motivated, well-organized, and technically proficient Senior Research Associate to join our Multi-Omic Technology Center, where you’ll work at the cutting edge of genomic technologies including emerging platforms like Ultima sequencing. In this hands-on role, you’ll be instrumental in scaling Arc Institute’s genomic capabilities, working directly with world-class scientists and investigators to enable breakthrough research. You’ll have the opportunity to master multiple sequencing platforms, shape workflows that impact the entire institute, and become a go-to expert in a collaborative, innovation-driven environment.

About You

You love science and learning. Whether it’s gaining knowledge in new fields of scientific research or learning a new lab technique, you never stop being curious and routinely enjoy stepping out of your comfort zone to learn new things.
You are flexible and adaptable, eager to try new ways of tackling problems beyond the approaches with which you’re familiar while also bringing energy and curiosity to the optimization of existing approaches.
You can work fast and are detail-oriented. You are careful and diligent about good documentation practices and keeping things organized while moving at a rapid pace.
You show initiative and can effectively work independently while also adapting well to situations where collaboration and communication with other RAs / Scientists will bring the best results.
You love being at the bench and are comfortable carrying out the routine execution of tasks while identifying opportunities to troubleshoot and improve bottlenecks.
Your organizational skills enable you to manage multiple concurrent projects, and your curiosity and creativity drive you to continuous learning and innovation.

In this position, you will

Work with both established and emerging sequencing technologies at the forefront of genomics innovation
Scale up genomic sequencing capabilities to meet growing internal demand
Contribute to the integration and optimization of new Ultima sequencing platforms into production-level workflows and ramp up throughput operations to reach maximum capacity across multiple instruments
Onboard and validate new sequencing platforms, ensuring seamless process integration
Support large institutional genomic initiatives through efficient workflow execution and quality management
Drive continuous improvement of data integration workflows and laboratory procedures
Expand your knowledge through exposure to multiple therapeutic areas and research applications across Arc’s diverse portfolio
Build your reputation as a subject matter expert in high-throughput genomics operations and platform management

Job Responsibilities

Perform NGS library management, pool strategies, and quality evaluation; manage sequencing submissions
Execute sequencing operations on multiple platforms and perform library preps for bulk and single-cell workflows
Work with scientists to explore, evaluate, and run proof of concept genomics technologies and assays, and generate data
Contribute to the implementation and optimization of LIMS system for sample tracking and data collection
Onboard and validate new sequencing platforms and manage process integration
Train graduate students, scientists, and junior RAs on various protocols and sequencing instruments, and help troubleshoot experiments
Maintain an accurate and detailed laboratory documentation
Write, update, and maintain Standard Operating Procedures (SOPs).
Effectively document and communicate results
Support routine lab activities, e.g. maintaining equipment, ordering/receiving supplies
Perform other duties as assigned and contribute to a collaborative, high-quality lab culture
Summarize and present results within and outside of the Genomics platform group

Requirements

BS/MS or equivalent professional experience in genomics, molecular biology, biochemistry, biology or related field
5+ year(s) of relevant post-graduate experience, preferably in the biotechnology/pharmaceutical industry with at least 3 years in a clinical diagnostics, biotech or research lab setting
Firm understanding of fundamental molecular biology concepts
Hands-on experience with basic molecular biology and QC techniques including nucleic acid extraction, purification and quantification (using Bioanalyzer, Tapestation and Qubit), PCR/RT-PCR, qPCR.
Extensive expertise in NGS technologies and workflows, including library preparation and sequencing (in particular the Illumina or Ultima platform)
Experience with high-throughput molecular workflows
Experience with LIMS/ELN systems
Strong organizational, documentation and analytical skills and attention to detail
Strong drive for excellence and self - self-starter
Demonstrated problem solving skills and ability to troubleshoot technical issues
Strong oral and written communication skills
Strong interpersonal skills and team player
Ability to work with minimal to moderate supervision in a dynamic environment and under tight deadlines

Preferred Qualifications

Experience with single-cell RNA-sequencing using the 10x Genomics or other platforms
Experience with processing mammalian cells and tissues
Experience with automation platforms

The base salary range for this position is $87,500 to $107,500. These amounts reflect the range of base salary that the Institute reasonably would expect to pay a new hire or internal candidate for this position. The actual base compensation paid to any individual for this position may vary depending on factors such as experience, market conditions, education/training, skill level, and whether the compensation is internally equitable, and does not include bonuses, commissions, differential pay, other forms of compensation, or benefits. This position is also eligible to receive an annual discretionary bonus, with the amount dependent on individual and institute performance factors.

","hiringOrganization":{"@type":"Organization","name":"Arc Institute","sameAs":"https://www.arcinstitute.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Palo Alto, CA","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":48,"item":{"@type":"JobPosting","title":"Graduate Research Associate, Post Bachelors","datePosted":"2025-09-17","description":"

Savannah River National Laboratory (SRNL) is inviting applications for the position of Post Bachelor’s Graduate Research Associate. The Graduate Research Associate will provide full-time, year-round technical support to a wide variety of projects through participation and collaboration with multidisciplinary engineering and research teams. The successful candidate will join a dynamic custom equipment development organization creating innovative solutions for the Savannah River Site, DOE complex and national security missions. Searching for creative, flexible, and self-motivated individuals to develop one-of-a-kind engineering solutions in a safe and responsible manner. Initial focus will be on X-Ray Imaging systems, technique development and service to SRS customers including training.

We are seeking a Graduate Research Associate to focus on X-ray Imaging Research and Development. In this position, the candidate will be expected to organize and execute research activities related to x-ray imaging through experimentation and/or simulation. This will include conducting research, documenting findings, and communicating outcomes with relevant project and program teams.

Candidate should be self-motivated, dynamic researcher willing to actively promote a collaborative, interdisciplinary research environment in x-ray imaging
Candidate should possess a background and working knowledge of x-ray imaging. They should exercise judgment with practical engineering or scientific principles to determine an appropriate action.
The Researcher will be expected to interface with and develop an externally funded project portfolio aligned with SRNL mission. This will include leading and partnering on proposal teams as well as managing both technical and programmatic aspects of successfully won projects.
Works safely with particular attention to quality. Complies with all policies and standards.
X-ray Imaging areas of interest may include technique development, system or sensor development, simulation and modelling for radiography, CT reconstruction algorithm development, etc.
Specifically sought-after skills include using Monte Carlo simulation for radiography, camera/scintillator development and deployment, and algorithm development with GPUs.
Works well in a collaborative, multi-disciplinary team environment. Generates original ideas and conveys them effectively through strong written and oral communication.
Maintaining a national presence at technical meetings - both internal to DOE and through professional organizations – is expected in the course of work.
Contribute to portions of journal papers, reports, software, proceedings, scientific and technical products. May contribute to the development of intellectual property leading to publications, copyrights and/or patents.
Effective written and oral communication is required for this position as well as strong interpersonal skills and the ability to collaborate effectively on diverse, multidisciplinary teams.
Work to broaden and deepen own technical knowledge and skills.
Lead subtasks and contributes to the production of technical reports, scientific and technical products, and journal papers in support of principle investigators and project managers.
Ability to develop internal and external scientific networks.

Minimum Qualifications

Candidates must have received a Bachelor’s degree within the past 24 months or within the next 8 months from an accredited college or university.
USD $65,000 annual salary
Immediate eligibility for Tuition Reimbursement Program up to $10,000/yr.
You will be provided, if you plan to relocate, in accordance with the BSRA Relocation Attachment, a $5,000 miscellaneous expense allowance (less applicable taxes) and a household goods move up to 20,000 pounds. All efforts will be made to provide the miscellaneous allowance payment within 2 payroll cycles after your start date, provided the relocation acknowledgement and repayment agreements have been returned to your recruiter. If there are any questions after reviewing the Relocation Attachment, please call me.
For ability to obtain and maintain a security clearance, US Citizenship is Legally Required

Benefits & Salary:

Preferred Qualifications

Proficient computer skills and a working knowledge of software packages, including Adobe Acrobat, Microsoft Suite: Word, Excel, Outlook, and PowerPoint.
Preferred Degrees: Mechanical, Electrical, Nuclear or Metallurgical Engineering along with Physics.
Graduate degree or working toward advanced degree.
Classwork or professional experience with x-ray imaging.
Experience developing AI/ML tools.
Simulation experience using MCNP, GEANT4, etc.
Experience with optics, cameras and scintillators.
Cross-discipline knowledge in scientific or engineering concepts
Active DOE clearance

","hiringOrganization":{"@type":"Organization","name":"Savannah River National Laboratory","sameAs":"https://www.srnl.gov/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Aiken, SC, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":49,"item":{"@type":"JobPosting","title":"LSW Care Manager - Population Health - Alexandria","datePosted":"2025-09-17","description":"

Schedule: Full Time – 80 hours/pay period – Monday to Friday – 8 a.m. to 4:30 p.m.

As a LSW Care Manager, you’ll be at the heart of our community, guiding and supporting at risk clients on their journey to wellness and independence. Whether coordinating personalized care plans, connecting clients with the care and services needed, advocating for client needs, or collaborating with healthcare teams, you’ll play a key role in delivering whole-person care that enhances quality of life, safety, and overall well-being for our clients. You’ll play a key role in ensuring a seamless and holistic approach to aging care clients need to live with dignity, independence, and wellness.

At Vivie, we value our people and offer a competitive pay range of $28.00/hr. to $31.50/hr. (hourly non-exempt) based on qualifications, experience, and location. Our comprehensive benefits package includes health coverage, grief support resources, and professional development opportunities.

Let’s grow together—apply now and discover the difference you can make at Vivie!

As a LSW Care Manager, you will:

Support Client Wellness and Implement Comprehensive Care Planning – Evaluate clients and caregivers for well-being, environmental concerns, and social determinants of health. Through thorough assessments you will evaluate client strengths, needs, and preferences to develop and implement personalized care plans that promote effective education, self-management, wellness and timely care delivery. Translate client needs into actionable goals and connect them with resources and tools to support their agreed-upon ideals. Implement social and clinical pathways. Assist in programming and collaborating with population health strategies to improve health outcomes for aging and at-risk communities.
Coordinate Care and Support Networks – Collaborate with healthcare providers, community-based organizations, and the client’s care network to ensure a coordinated, high-quality care experience. Facilitate appropriate referrals and connections to promote effective education, self-management, enhance cost-effectiveness, quality outcomes and timely service delivery. Manage and monitor the ongoing provision and need for care delivery to promote optimal health and financial outcomes. Support at-risk clients with aging care and service needs, fostering engagement and coordination across multiple health and community-based entities. Assist in implementing remote patient monitoring equipment.
Client Advocacy and Professional Support – Act as an advocate for clients by ensuring their healthcare needs are met and minimizing fragmentation in the healthcare delivery system. Uphold professionalism by maintaining legal and ethical standards, privacy requirements, and professional boundaries.
Other Duties as Assigned – The duties and responsibilities listed above are representative of the nature and are not necessarily all inclusive.

This Job Also Requires:

Bachelor’s degree in social work or a related field is desired, or at least five years’ experience in care management.
Current certification in care management is preferred, or willingness to obtain certification within one year of hire.
Experience working with aging populations, understanding geriatric care, and familiarity with health and social resources are highly valued.
Proficiency in basic medical terminology and the ability to interpret clinical and social information.
Ability to pass state mandated background checks.
Experience working with aging populations, understanding geriatric care, and familiarity with health and social resources are highly valued.
Proficiency in basic medical terminology and the ability to interpret clinical and social information.
Valid driver's license and access to insured personal vehicle.
Physical capability to perform job duties.
Ability to read, write, and speak English to communicate effectively with staff, patients, families, and external partners.

Additional Details:

Employment Type: Hourly, non-exempt (eligible for overtime)
Department: Social Services
Leadership Received: Director of Care Management & Integration and Lead Care Manager
Division: Population Health
Travel Requirements: Yes
This role does not include supervisory responsibilities

","hiringOrganization":{"@type":"Organization","name":"Vivie","sameAs":"https://vivie.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Alexandria, Minnesota, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":50,"item":{"@type":"JobPosting","title":"Certified Population Health Pharmacy Technician - Full-Time - Day","datePosted":"2025-09-17","description":"

Schedule

Full-Time: 40 Hours/Weekly

M-F 8-430

General Summary

Supports the pharmaceutical management efforts across the continuum of care from utilization management to care management to adherence for value-based care populations served through WellSpan Population Health Services (WPHS). This role utilizes Epic and other resources to gather needed information for other team members while assuring excellence in the patient and provider experience. While some aspects of the role are highly regulated there are many opportunities for innovation for which this team member will be uniquely positioned to influence.

Remote Work Capableessential Functions:

Receives and prepares information, gathers new information, and completes in collaboration with utilization management (UM) team members through Epic for authorization requests.
Manages and assists in communications to physician offices/pharmacies/members/other departments to obtain additional information and to keep physicians/pharmacies/members aware of current authorization status. This work will be conducted with a focus on an exceptional customer experience.
Collaborates with care management team members and others in the WellSpan Health system including patient outreach to achieve adherence goals established within value-based and pay-for-performance programs. This effort includes monitoring reports, performing patient/provider outreach, and assuring accuracy of information in data sources.
Retrieves information and builds reports as needed from various sources to support the efforts of utilization management and success in value-based care.
Collaborates with WPHS customer service team members and the pharmacy benefit manager to assist members in understanding and navigating the processes for utilizing their health plan or other contracted benefits.
Assists in utilization management and care management improvement efforts (development, establishment, implementation of goals, objectives, policies, and procedures) leveraging the LDMS process. This includes receiving complaints/issues elevated from other sources outside of the department.
Performs member outreach activities related to adherence with a focus on achieving the best health outcome for members while contributing to quality performance success.

Common Expectations:

Maintains established policies and procedures, objectives, quality assessment, and safety standards.
Maintains personal professional growth and development.
Maintains a balance of productivity, quality, and timeliness of job accountabilities. Participates in department self-audit or other compliance procedures.

\n\n

Qualificationsminimum Education:

High School Diploma or GED Required
Bachelors Degree Preferred

Work Experience:

2 years Retail or other experience as a pharmacy technician. Required
1 year Experience in third-party administration pharmacy management, utilization or care management, health plan benefits, or a role in a pharmacy benefit manager or health plan. Preferred

Licenses:

Certified Pharmacy Technician Upon Hire Required

Courses And Training:

Health Plan related certifications (e.g., billing and reimbursement, medication therapy management, medication history) Upon Hire Preferred

Knowledge, Skills, And Abilities:

Collaborative, displaying skill in seeking partners to accomplish goals.
Excellent communicator in individual and group settings.
Displays a willingness to learn from others with a mindset of personal self-awareness.
Growing skills at critical thinking in a clinical setting.
Independent worker able to take direction and complete tasks with minimal supervision.
Self-directed learner and problem-solver.

Benefits Offered:

Comprehensive health benefits
Flexible spending and health savings accounts
Retirement savings plan
Paid time off (PTO)
Short-term disability
Education assistance
Financial education and support, including DailyPay
Wellness and Wellbeing programs
Caregiver support via Wellthy
Childcare referral service via Wellthy

\n\nWellSpan Health’s vision is to reimagine healthcare through the delivery of comprehensive, equitable health and wellness solutions throughout our continuum of care. As an integrated delivery system focused on leading in value-based care, we encompass more than 2,300 employed providers, 250 locations, nine award-winning hospitals, home care and a behavioral health organization serving central Pennsylvania and northern Maryland. Our high-performing Medicare Accountable Care Organization (ACO) is the region’s largest and one of the best in the nation. With a team 23,000 strong, WellSpan experts provide a range of services, from wellness and employer services solutions to advanced care for complex medical and behavioral conditions. Our clinically integrated network of 3,000 aligned physicians and advanced practice providers is dedicated to providing the highest quality and safety, inspiring our patients and communities to be their healthiest.","hiringOrganization":{"@type":"Organization","name":"WellSpan Health","sameAs":"https://www.wellspan.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"York, PA, United States","addressCountry":"United States","addressRegion":"North America"}}}}]}

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