{"@context":"https://schema.org","@type":"ItemList","name":"Research Associate Job Description and Opportunities","description":"Explore the role of a Research Associate, responsibilities, required skills, and career prospects. Find Research Associate positions on top job boards.","itemListElement":[{"@type":"ListItem","position":1,"item":{"@type":"JobPosting","title":"Postdoctoral Research Associate","datePosted":"2025-09-24","description":"

Grade UE07 £41,064 – 48,822 per annum

CSE / School of Mathematics

Full time: 35 hours per week

Fixed term: 36 months (with possible extension to 48 months)

\n\n\n\n

We are looking for a talented and ambitious early career researcher to work on the project “Numerical Analysis for Stable AI” funded by a European Research Council Advanced Grant.

\n\n

The Opportunity:

This postdoctoral position will be devoted to research on algorithms in Artificial Intelligence (AI) from the perspective of numerical analysis and computational mathematics. The overarching aim of the project is to develop new mathematical theory and algorithms to identify, quantify and, where possible, mitigate the empirically observed vulnerabilities in current AI systems. The project is led by Professor Des Higham in the School of Mathematics at the University of Edinburgh, and it will exploit links with EPCC (formerly the Edinburgh Parallel Computing Centre), the Generative AI Lab, and the Centre for Technomoral Futures.

The successful candidate will contribute to both theoretical analysis and computation experimentation (in Python, using GPUs), with the precise balance determined by the candidate’s background and interests. The mathematical tools involved will include matrix analysis, optimization, backward error analysis, condition number theory, high-dimensional analysis (concentration of measure) and stochastic computation.

A record of some high-quality mathematical reports and/or publications, as well as coding skills (e.g. in MATLAB, Python, C) are essential. You will also closely collaborate with a second postdoctoral researcher, who will be hired later in the year, a cohort of PhD students, and a range of visiting experts. Communication skills are essential for this project, as the results will be developed in collaboration with AI developers, end-users, and regulators, and with feedback from colleagues in ethics, law, social science and the creative arts.

You will be part of Edinburgh’s world-leading Applied and Computational Mathematics Group, providing a friendly and vibrant research environment. You will also have access to a generous travel allowance which will enable you to present your work at national and international conferences. There is scope for a strong candidate to shape the research direction.

\n\n

Your skills and attributes for success:

Research experience and some publications in at least one of numerical analysis/scientific computing and/or algorithms for AI
Enthusiasm to investigate and quantify vulnerabilities in current AI systems
Excellent academic writing and communication skills
Strong coding skills in at least one of MATLAB, Python, C, and experience with, or willingness to learn, Pytorch and GPUs

\n\n

Click to view a copy of the full job description (opens new browser tab)

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Applicants should upload a CV and a one page summary of their previous research contributions when applying for the post online. In addition, they should provide details of two referees whom we may contact for letters of reference.

For informal enquiries about the post please contact Des Higham – d.j.higham@ed.ac.uk

\n\n

As a valued member of our team you can expect:

A competitive salary.
An exciting, positive, creative, challenging and rewarding place to work.
To be part of a diverse and vibrant international community.
Comprehensive Staff Benefits, such as a generous holiday entitlement, competitive pension schemes, staff discounts, and family-friendly initiatives. Check out the full list on our staff benefits page (opens in a new tab) and use our reward calculator to discover the total value of your pay and benefits.

\n\n

Championing equality, diversity and inclusion

The University of Edinburgh holds a Silver Athena SWAN award in recognition of our commitment to advance gender equality in higher education. We are members of the Race Equality Charter and we are also Stonewall Scotland Diversity Champions, actively promoting LGBT equality.

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Prior to any employment commencing with the University you will be required to evidence your right to work in the UK. Further information is available on our right to work webpages (opens new browser tab).

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The University may be able to sponsor the employment of international workers in this role. This will depend on a number of factors specific to the successful applicant.

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Key dates to note

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The closing date for applications is 15th October 2025.

Unless stated otherwise the closing time for applications is 11:59pm GMT. If you are applying outside the UK the closing time on our adverts automatically adjusts to your browsers local time zone.

We anticipate that interviews will be held in the week November 17, 2025.

\n\nAs a world-leading research-intensive University, we are here to address tomorrow’s greatest challenges. Between now and 2030 we will do that with a values-led approach to teaching, research and innovation, and through the strength of our relationships, both locally and globally.","hiringOrganization":{"@type":"Organization","name":"The University of Edinburgh","sameAs":"https://www.ed.ac.uk/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":2,"item":{"@type":"JobPosting","title":"Research Associate II, S3","datePosted":"2025-09-24","description":"Purpose of the Position:\n\n

Perform funded research and provide on-site support to the Army in the role of Operations Coordinator (Ops Cor).
Duties/Responsibilities
• Perform funded research and provide on-site support to the Army in the role of Operations Coordinator (Ops Cor)
• Provide support to DASA DEC organization, perform logistics, cost analysis, and contract preparation tasks and duties
• Mentor undergraduate students in the area of military support

\n\n\n\nMinimum Requirements:\n\n

• Bachelor's degree preferably in Science, Engineering or Business with 18 - 21 months (1.5 - 1.75 years) of full-time work experience
• 6+ months on-site support of the Army
• 3+ months conduct cost analysis for the Army
• US citizenship is required

\n\n\n\nDesired Qualifications:\n\n

• Bachelor's degree with 24+ months (2+ years) of full-time work experience preferred
• 9+ months on-site support of the Army desired.
• Development of RSCA (Request for Services of Contract Approval) packages and assisting in the development of IGCEs (Government Contract Estimates) preferred

\n\n\n\nPublished Salary (if available):\n\n

$52,500 - $56,200

","hiringOrganization":{"@type":"Organization","name":"The University of Alabama in Huntsville","sameAs":"https://www.uah.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Alabama","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":3,"item":{"@type":"JobPosting","title":"Research Associate – IIM Bangalore Center of Excellence for Digital Public Goods","datePosted":"2025-09-24","description":"

Ref: IIMB/RA/RECT/2025/56 Date: 24 September 2025

\n\n\n\nAbout IIMB\n\n

The Indian Institute of Management Bangalore (IIMB) is a leading graduate school of

management in Asia. Under the IIM Act of 2017, IIMB is an Institute of National Importance.

\n\n\nIndustry/Service\n\n

Higher Education

\n\n\nPosition\n\n

Research Associate – IIM Bangalore Center of Excellence for Digital Public Goods

\n\n\nPurpose\n\n

IIM Bangalore's Center of Excellence for Digital Public Goods (CDPG) is seeking highly motivated and talented Research Associate to join our team. The Center of Excellence for Digital Public Goods at IIM Bangalore is a leading institution dedicated to studying and advancing digital public infrastructure (DPI) and digital public goods (DPG) initiatives. As a repository of knowledge in this field, we provide thought leadership and advisory services for policymakers, practitioners, and researchers worldwide. Our rigorous research evaluates the effectiveness of DPI and DPG initiatives, positioning us as a trusted authority on digital public infrastructure and digital public goods. For more details, please visit the CDPG website at www.iimb.ac.in/cdpg. As a Research Associate, you will play a crucial role in leading cutting-edge research, developing innovative solutions, and contributing to the overall vision of the center.

\n\n\nDuration\n\n

Initially for a period of 6 Months. Based on the performance and requirement, it can be extended further.

\n\n\nReporting to\n\n

Prof. R Srinivasan

\n\n\nPrincipal Accountabilities & Responsibilities\n\n

Conduct research: Support research on digital public goods, with a focus on building an inclusive and open data repository, and documenting success stories of DPI and DPG initiatives leading to a one-of-its-kind knowledge repository.
Data analysis and interpretation: Collect, analyse, and interpret data related to digital public goods, utilizing appropriate research methodologies and statistical techniques.
Project development: Contribute to the development of research projects and proposals that align with the center's objectives, including in evangelizing and documenting international and national replications of DPI and DPGs in other contexts.
Partnerships and fund raising: Assist in securing funding for research initiatives and establishing partnerships with relevant stakeholders.
Publication and dissemination: Contribute to research papers, reports, and other publications for dissemination in reputable academic journals, conferences, and policy forums. Contribute to the center's data repository, knowledge repository, and experience repository through collaborative documentation and knowledge sharing.
Collaborative engagement: Collaborate with researchers, practitioners, policymakers, and industry experts to foster interdisciplinary research collaborations and contribute to the overall intellectual environment of the center.

\n\n\nQualification and Personal Profile\n\n

A Masters’ degree in a relevant field such as management, information systems, public policy, economics, or a related discipline.
Strong research background with a focus on digital technologies, open source software, data governance, or related areas.
Expertise in research methodologies, data analysis, and statistical techniques, and/ or qualitative research methods.
Excellent written and verbal communication skills to effectively communicate research findings and engage in collaborative discussions.
Ability to work independently as well as part of a team, with strong organizational and time management skills.

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

Key Skilland Ability Requirements

\n\n

Knowledge of, and experience in working with emerging technologies, digital innovation, and the concept of digital public goods.
Prior experience in working in research institutions/ research centres.

\n\n\n\n

The closing date for applications is 08 October 2025. Only shortlisted candidates will be intimated. All fields in the application form are mandatory, and the following documents are required to be uploaded while submitting the application.

10th & 12th Marksheets.
Diploma/Graduation - All semester wise Marksheets & Final Diploma/Degree Certificate.
Masters/Post-Graduation - All semester wise Marksheets & Final Degree Certificate.

Applications without these documents will be treated as incomplete and will not be considered.

Interested candidates may fill out the application using the link: here

\n\n\n The Indian Institute of Management Bangalore (IIMB) is a leading graduate school of management in Asia. Under the IIM Act of 2017. IIMB is an Institute of National Importance.\n\n\n
\n\n\n IIMB has 113 full time faculty members, about 1200 students across various degree-granting programmes and nearly 5000 annual Executive Education participants.\n\n\n
\n\n\n Our logo carries a proclamation in Sanskrit, तेजस्वि नावधीतमस्तु (tejasvi navadhitamastu), which translates as ‘let our study be enlightening’.\n\n\n
\n\n\n Our vision is to be a global, renowned academic institution fostering excellence in management, innovation and entrepreneurship for business, government and society.\n\n\n
\n\n\n We have taken several steps to meet the vision set for IIMB. These include hiring high quality faculty, enhancing the quality of research, emphasizing internationalization, expanding our activities in the field of entrepreneurship, in both research and mentoring, scaling up in terms of student intake in all the programmes, deepening our engagement with the alumni, improving infrastructure, and improving administration and governance.","hiringOrganization":{"@type":"Organization","name":"Indian Institute of Management Bangalore","sameAs":"https://www.iimb.ac.in/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bangalore, India","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":4,"item":{"@type":"JobPosting","title":"Research Associate - Neural Plasticity","datePosted":"2025-09-24","description":"

Description

A Little About Us:

The Lieber Institute for Brain Development (LIBD) was established in 2010 to plot a new course in biomedical research that would change the lives of individuals affected with developmental brain disorders. We are one of the only research institutions in the world focused specifically on understanding how genes and the environment influence the way our brains develop that lead to conditions such as schizophrenia, autism, bipolar disorder and related developmental brain disorders. Through our cutting-edge research, answers are emerging and being translated into a robust pipeline of new drugs in development. And, by focusing on genes and their dynamic interplay with the environment, we are getting even closer to the “holy grail” in medical research, the discovery of strategies for primary prevention.

We are a group of dedicated, multidisciplinary and optimistic researchers, working at the cutting edge of science, utilizing state-of-the-art tools to unlock the mystery of the brain and transform the way we approach the development of new treatments, and ultimately cures. LIBD is an independent 501(c)(3) medical research institute located in the Bioscience Park on the campus of the Johns Hopkins School of Medicine and Hospital in Baltimore, MD.

Job Summary:

We are seeking an enthusiastic and self-motivated individual to join our group as a Research Associate. This position is best suited for candidates with significant experience in molecular biology, next generation sequencing, library prep, FACS sorting, and microscopy. The successful applicant will work within a dynamic team-based environment in a translational research setting with a focus on spatial transcriptomics projects in postmortem human brain tissue. Projects aim to generate transcriptome-scale maps in the human brain to understand differences in spatial gene expression in neuropsychiatric disorders. The Research Associate will thoughtfully conduct experiments, analyze data, participate in experimental design, and train junior personnel

Overview Of Duties:

Assist with brain tissue dissections
Cryosectioning postmortem human brain tissue
RNA extraction and qPCR
RNA-seq library construction
Nuclei isolation and FACs sorting
Immunocytochemistry and single-molecule fluorescent in situ hybridization
Confocal microscopy and slide scanning
Data analysis in MATLAB and R programming languages

*This position description is intended to serve as a summary of the general purpose and essential functions of this position. It may change as circumstances warrant and may include other duties as deemed necessary by management.

Requirements

Professional And Education Requirements:

A B.S. degree in Neuroscience, Biology, or a closely related field is required. MS degree is preferred
Minimum 3 years of related laboratory research experience, including experience with RNA-seq is required

Familiarity with any of the following is a plus:

O Neuroanatomy

O Confocal Microscopy

o Programming in MATLAB, R or Python

Required Special Knowledge, Skills and Abilities:

Attention to detail and the ability to perform work carefully and efficiently is essential.
Ability to execute experiments independently
Ability to participate in experimental design and data analysis
Willingness to follow detailed technical protocols
Excellent organizational and communication skills

*Applicants must currently be authorized to work in the U.S. on a full-time basis. Employment-based visa sponsorship (including H-1B sponsorship) is not available for this position.

Physical Requirements:

Remaining in a seated or standing position for extended periods of time;
Reaching and grasping to manipulate objects with fingers;
Mobility, including the ability to maneuver around a laboratory setting including the ability to move materials weighing up to 25 pounds;
Communication skills using the spoken and written word;
Having the ability to receive detailed information through oral communication;
All other physical demands in a standard laboratory environment.

** If accommodations are needed due to pregnancy or a disability, please contact jobs@libd.org.

Compensation

Candidates are hired within the starting salary range for the position which is the lower portion of the overall range. The starting salary range for this position is $52k - $55k with opportunities for employee growth over time. Placement in the starting range is based on job-related skills and experience, as evaluated throughout the interview process.

Benefits

The Lieber Institute for Brain Development offers a competitive, comprehensive benefits package to help us attract and retain the best talent. Please visit https://www.libd.org/careers/benefits/ for more information.

EEOC Statement: At the Lieber Institute, we are committed to a work environment of mutual respect where employment decisions are based on merit. As an equal opportunity employer, the Lieber Institute does not discriminate in employment opportunities on the basis of race, color, religion, color, sex, gender identity/expression, sexual orientation, pregnancy, marital status, age, national origin or ancestry, citizenship, disability (physical or mental), genetic information, military service, or other non-merit based factors protected by state or federal law or local ordinance, with regard to any position or employment for which the applicant or employee is qualified.

LIEBER INSTITUTE FOR BRAIN DEVELOPMENT'S COMMITMENT TO DIVERSITY, EQUITY, AND INCLUSION

The Lieber Institute for Brain Development is a transparent and collaborative community working to produce unique and imaginative patient-oriented solutions to developmental neuropsychiatric disorders. It is committed to integrating scientists from diverse disciplines, cultures, and countries into a research team that draws upon the best of its staff. The Institute is historic—it is defining a unique model for ground-breaking science. It values translational science that revolutionizes the field and improves the quality of life for those affected by mental illness. The Institute provides an environment that fosters independent growth through mentorship and a supportive, collegial community. Diverse minds, ideas, and talent are needed to support LIBD's mission. Fresh, innovative ideas and perspectives are a competitive necessity in an increasingly diverse and global marketplace. The success of the Institute's mission depends upon leveraging a diversity of talent.

The Institute's commitment to diversity goes beyond compliance with laws and regulations that promote equal employment opportunity, prohibit discrimination and harassment, and support minority and woman owned businesses. To realize the advantages of its diversity, it is necessary to work effectively together even when differences challenge us to consider ideas and methods that seem impractical or make us feel uncomfortable.

The Lieber Institute for Brain Development demonstrates its commitment to diversity by:

Including others: Talent is not limited to those with a narrow set of industry and academic credentials. The Institute is committed to building diverse teams, inviting others to share their perspectives, seeking out a diversity of input when making decisions, questioning traditional thinking, and promoting continuous learning and development.
Respecting one another: The Institute is committed to listening carefully to others, seeking consensus, engaging in active and constructive debate, thoughtfully challenging one another, and providing constructive feedback.
Building trust: The Institute is committed to sharing information and resources, depending on one another to get things done, keeping promises, and conveying high integrity in all actions.

","hiringOrganization":{"@type":"Organization","name":"Lieber Institute for Brain Development","sameAs":"https://www.libd.org/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Baltimore, MD, US","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":5,"item":{"@type":"JobPosting","title":"Research Associate","datePosted":"2025-09-24","description":"

Drive innovation in traffic video analytics by building and optimising cutting-edge computer vision models that improve road safety and transport planning.

Full-time appointment on a fixed term basis for two years.

Base salary range: Level A, $83,499– $112,371 p.a. (pro-rata) plus 17% superannuation.

About The Area

Join the Planning and Transport Research Centre (PATREC) at UWA, where cutting-edge research meets real-world impact. RoadSense Analytics (RSA) is a next-generation video analytics platform for traffic analysis, representing seven years of continuous R&D. It transforms pioneering Australian research into a market-ready product for transport planning.

About The Opportunity

Design, test, and refine computer vision models for traffic video analytics, including detection, tracking, segmentation, and post-processing tasks.
Prepare and manage datasets, benchmark and evaluate emerging frameworks, and contribute to deployment testing and optimisation across varied environments.
Work within a small, innovative team to document findings, produce technical outputs, and translate research into real-world impact on road safety and transport planning.

About You

Tertiary degree in Computer Science, Applied Mathematics/Statistics, Robotics, Physics or related discipline, with an excellent academic record.
Strong foundations in applied mathematics, computer vision and machine learning, particularly object detection and tracking.
Proficiency in deep learning frameworks (e.g., PyTorch, TensorFlow) and Python ML libraries (e.g., NumPy, OpenCV, scikit-learn).
Experience with dataset preparation, training pipelines, and evaluation methods.
Ability to work both independently and collaboratively in a research team.

Position description: PD [Research Associate] [521359].pdf

To learn more about this opportunity, please contact Associate Professor Chao Sun at chao.sun@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.

You may submit a statement describing any personal circumstances relevant to your application. This can include academic/professional interruptions or achievements relative to opportunity.

Closing date: 11:55 PM AWST on Wednesday, 22 October 2025

Note: We encourage you to submit your application as soon as possible, as we may begin reviewing candidates while the position remains open.

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.

","hiringOrganization":{"@type":"Organization","name":"The University of Western Australia","sameAs":"https://www.uwa.edu.au/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Perth, Crawley","addressCountry":"Australia","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":6,"item":{"@type":"JobPosting","title":"Securities Research Associate","datePosted":"2025-09-24","description":"

Job Description

About This Role:

Wells Fargo is seeking a Securities Research Associate

The role involves working closely with the US deal team on M&A deal executions, pitchbooks, valuations, peer analysis, opportunity analysis, and other industry-related materials, with significant opportunities to learn, develop and work as an integral member of the business.

In This Role, You Will:

Provide support in the editing and publishing functions within the Global Research and Economics Group in Wells Fargo Securities
Generate research packet products, post research documents to market data vendors, update and maintain mailing lists, and provide client access to web sites
Assign reports to Editors and Supervisory Analysts to ensure the most efficient use of resources
Maintain databases
Receive direction from leaders
Exercise independent judgment while developing the knowledge to understand function, policies, procedures, and compliance requirements
Collaborate and consult with peers, colleagues and managers to resolve issues and achieve goals

Required Qualifications:

2+ years of Securities Research experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education

Desired Qualifications:

Work on various work streams that form key components of M&A Buy or Sell side deals
Assist in preparing Pitch books, including industry overviews, company profiles, strip profiles, management biographies, brokers' outlook, share price performance, deal case studies, evolution of industry/peer valuation multiples, possible buyer/seller opportunities
Work on comparable company analysis, precedent transaction analysis, buyer or target identification, company/M&A screening and newsletter preparation
Work on financial analysis, industry benchmarking and valuation models (DCF, LBO, football field, merger model and analysis)
Develop an understanding of key M&A drivers and trends and M&A market activity
Work independently on complex projects and deliver high quality deliverables
Effectively communicate with key stakeholders in the US

Job Expectations:

Ability to proficiently use Microsoft Office applications, especially Power Point and Excel
Knowledge of database tools – FactSet, Merger market, Dealogic, Thomson One, Capital IQ, Factiva, and Bloomberg
Impeccable communication and interpersonal relationship skills with the ability to interact with senior professionals and key stakeholders
Strong time management skills and ability to work under pressure and meet strict deadlines
Attention to detail and ability to ensure high quality of deliverables
Ability to provide innovative ideas to efficiently execute the tasks
Ability to identify proactive ways to contribute to firm's goals & mission
2+ years of experience. Strong knowledge of accounting and financial concepts. Knowledge of investment banking concepts including M&A as a product will be an added advantage
Outstanding academic qualifications – MBA, CA or MS Finance from a premier institute. CFA is an advantage

Posting End Date:

29 Sep 2025

*Job posting may come down early due to volume of applicants.

We Value Equal Opportunity

Wells Fargo is 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 legally protected characteristic.

Employees support our focus on building strong customer relationships balanced with a strong risk mitigating and compliance-driven culture which firmly establishes those disciplines as critical to the success of our customers and company. They are accountable for execution of all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable Wells Fargo policies and procedures, appropriately fulfilling risk and compliance obligations, timely and effective escalation and remediation of issues, and making sound risk decisions. There is emphasis on proactive monitoring, governance, risk identification and escalation, as well as making sound risk decisions commensurate with the business unit’s risk appetite and all risk and compliance program requirements.

Candidates applying to job openings posted in Canada: Applications for employment are encouraged from all qualified candidates, including women, persons with disabilities, aboriginal peoples and visible minorities. Accommodation for applicants with disabilities is available upon request in connection with the recruitment process.

Applicants With Disabilities

To request a medical accommodation during the application or interview process, visit Disability Inclusion at Wells Fargo.

Drug and Alcohol Policy

Wells Fargo maintains a drug free workplace. Please see our Drug and Alcohol Policy to learn more.

Wells Fargo Recruitment and Hiring Requirements:

Third-Party recordings are prohibited unless authorized by Wells Fargo.
Wells Fargo requires you to directly represent your own experiences during the recruiting and hiring process.

","hiringOrganization":{"@type":"Organization","name":"Wells Fargo","sameAs":"https://www.wellsfargo.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"111442-IND-BENGALURU-INTL BLR BLK B3 PETUNIA, India","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":7,"item":{"@type":"JobPosting","title":"Research Associate","datePosted":"2025-09-24","description":"

Long Description

Strong proficiency in SAS and R programming.

In depth knowledge in using Phoenix WinNonlin.

Advanced skills in multiple statistical areas.

Excellent interpersonal communication skills, verbal, and written English.

Advanced knowledge in statistical aspects of study design.

Experience working with or at Clinical Research unit

Experience with various regulatory regulations

Competencies

\n2. Innovation & Creativity5. Result Orientation6. Process Excellence7. CollaborationCustomer FocusTeamworkTime-Management

Education

\nMastersDoctorate in Statistics

Work Experience

Biostatistician having 3-6 years of experience in SAS & R Programming

","hiringOrganization":{"@type":"Organization","name":"Lupin","sameAs":"https://www.lupin.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pune LBC, MH, IN","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":8,"item":{"@type":"JobPosting","title":"Research Associate (Battery Energy Storage Systems)","datePosted":"2025-09-24","description":"

The Energy Research Institute @ NTU (ERI@N) distinguishes itself through research excellence directed towards outcomes of industry relevance. The focus is on system level energy research for tropical megacities. ERI@N is committed to building strong alliances with government agencies, leading industry players, SMEs and global universities to support Singapore’s sustainability objectives and energy transition. The Institute hosts Interdisciplinary Research Programmes, Flagship Programmes, an Accelerator Programme and the Standards Development Organization. The scope covers the energy value chain from energy generation to innovative end-use solutions.

We are looking for an innovative Research Associate to take on the anticipated challenges that face the largescale deployment of BESS in the future.

Key Focal Areas Include:

Control of BESS assets operating within unconventional electrical grids.
Modeling and simulation of BESS within large, interconnected networks.
Diagnostic methods to ascertain BESS state of health and remaining useful life.

Key Responsibilities:

Development of control methods to enhance BESS performance and provide ancillary grid services.
Modeling and simulation of BESS systems together with large grid models densely populated with inverter based generation / loads.
Testing of BESS systems in high power laboratory environment (1500Vdc, 350kW).
Assembly, commissioning and operation of BESS test facility. Includes PLC programming, HMI development, commissioning of instrumentation and measurement systems.
Development and verification of test methods to assess battery pack condition and remaining useful life.

Job Requirements:

Master’s degree in electrical engineering or related field
5 years of technical hands-on experience in the design, simulation and testing of power electronic converters and battery systems.
Familiarity with BESS standards including UL9540, UL1741, NFPA855 and IEC62933.
Good written and oral communication skills.
Proficiency in power electronic converter design, converter controls, grid integration and electrical power systems.
Proficiency in lithium-ion battery technology and testing at both the cell and pack level.
Familiarity with PLC and rapid controller prototyping (TwinCAT, NI cRIO, dSpace, Typhoon HIL)
Proficiency in circuit and system level simulation (Simulink, PSCAD, PLECS, PSS/E).
Ability to work independently and possess excellent organizational / time management skills.

We regret to inform that only shortlisted candidates will be notified.

Hiring Institution: NTU","hiringOrganization":{"@type":"Organization","name":"Nanyang Technological University","sameAs":"https://www.ntu.edu.sg/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"NTU Main Campus, Singapore","addressCountry":"Singapore","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":9,"item":{"@type":"JobPosting","title":"Postdoctoral Research Associate - Pharmaceutical Sciences - Yang Lab","datePosted":"2025-09-24","description":"A Postdoctoral Research Associate position is available in the Jun J. Yang Lab to study genomics and pharmacogenomics of childhood leukemia. Using state-of-the-art molecular profiling tools (e.g., single cell sequencing, spatial transcriptomics), we are interested in identifying both inherited and tumor genetic variations related to leukemia treatment response and toxicity. Functional and mechanistic studies utilizing preclinical models and clinical samples are critical components of the highly translational research program in this laboratory.

We are seeking an ambitious postdoctoral associate with a track record of productivity and strong interest in translational cancer research. Applicants should have a recent doctoral degree (PhD, MD, PharmD, or combined degrees). With a general background in pharmacology and genomics, the ideal candidate would be familiar with leukemia modeling and anti-leukemic drug evaluation in vitro and in vivo.

St. Jude Children’s Research Hospital, located in Memphis, Tennessee, is a premier center for research and treatment of potentially fatal childhood diseases, including cancer and certain blood, genetic, and immunodeficiency disorders. The hospital’s mission is to advance cures, and means of prevention, for pediatric catastrophic diseases through research and treatment. St. Jude is dedicated to providing unsurpassed patient care and to advancing the health of children through biomedical research.

St. Jude is an Equal Opportunity Employer

No Search Firms

St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

Position Title:

Postdoc Research Associate

Appointment Type:

Post Doc/Trainee

Job Description:

Summary Of Duties And Responsibilities:

The postdoctoral scholar will work in a team with two graduate students to develop these models. Please note that while we are a member of the Nanovaccine Institute, this project does not involve nanoparticle vaccine work.

Required Minimum Qualifications:

Phd
Experience conducting research in mammalian cell culture, molecular and cellular biology assays, and microscopy
Clean room microfabrication experience (photolithography)
Experience mentoring graduate and undergraduate students

Preferred Qualifications:

Experience with animal studies
Experience in DNA and/or RNA sequencing, immunostaining, and fluorescence in situ hybridization
Experience with in vitro models
Experience in protocol and manuscript development, and in grant writing

Department/Program & College Description:

The Kozminsky Lab develops and applies technology to create in vitro models of physiological microenvironments. Grounded in a high-throughput DNA-directed patterning technique, we are able to recapitulate cellular spatial arrangement at high throughput and high resolution. We are currently developing in vitro models to study prostate cancer metastasis to the bone marrow, with an emphasis on the study of tumor cell dormancy and osteoblastic/osteolytic phenomena.

Department Unit/Website: Https://Www.Cbe.Iastate.Edu/Mollykoz/

Proposed Start Date:

October 20, 2025

Proposed End Date Or Length Of Term:

October 19, 2028

Number Of Months Employed Per Year:

12 Month Work Period

Time Type:

Full time

Application Instructions:

To apply for this position, please click on “Apply” and complete the Employment Application. Please be prepared to enter or attach the following:
1) Resume/Curriculum Vitae
2) Letter of Application/Cover Letter
If you have questions regarding this application process, please email employment@iastate.edu or call 515-294-4800 or Toll Free: 1-877-477-7485.
Why Choose ISU?
Iowa State Postdocs enjoy comprehensive health and work-life benefits, including medical and dental; as well as:
• Retirement benefits including defined benefit and defined contribution plans
• Generous vacation, holiday, and sick time and leave plans
• Onsite childcare (Ames, Iowa)
• Flexible Spending Accounts
• Various voluntary benefits and discounts
• Employee Assistance Program
• Wellbeing Program

Original Posting Date:

September 24, 2025

Posting Close Date:

September 30, 2025

Job Requisition Number:

R17831","hiringOrganization":{"@type":"Organization","name":"Iowa State University","sameAs":"https://www.iastate.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"ATRB - Biosciences Facilities Advanced Teaching and Research Building, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":11,"item":{"@type":"JobPosting","title":"Clinical Research Associate - Trainee Program","datePosted":"2025-09-24","description":"

Assoc CRA Trainee Program Auckland New Zealand - now taking applications for our next intake commencing on the 12th January 2026

Ready to kickstart your career in clinical research? Join IQVIA, a global leader in driving healthcare forward, as a CRA Trainee! We're looking for critical thinking, detail-oriented, and proactive individuals with strong communication skills to join our fantastic CRA Training Program in Auckland New Zealand. Applications close Friday 3rd October.

This is your chance to gain the skills and knowledge to become a successful Clinical Research Associate. Our innovative and modular training program is customized to your experience level, combining classroom learning with hands-on experience, guided by experienced CRAs, Line Managers, and Quality Managers. Imagine yourself working for a Fortune 500 company, with world-class training and endless opportunities for growth! Many of our past trainees have gone on to exciting roles like Senior CRA, Clinical Project Manager, and Line Manager. Upon successful graduation from the training program, you will be assigned to studies as an IQVIA CRA in our Full Service model, or in our Flexible Resource model.

Our Cutting-Edge Training Program:

At IQVIA, we're committed to taking clinical research to the next level. Our CRA Training Program is designed with a performance-driven approach, equipping you with the technical and analytical skills to drive healthcare forward. Experience a flexible and engaging curriculum that simulates the life of a CRA, covering all phases of monitoring a clinical trial, including site selection, initiation, monitoring, and close-out. The program also includes:

Virtual learning activities: Interactive sessions designed to prepare you for real-world scenarios.
Web-based training: Scenarios and case studies to develop your decision-making skills.
Learning clinics: Collaborative learning opportunities to enhance your understanding.
On-the-job training: Practical experience to build your competence quickly.
Mentorship: Guidance from experienced professionals to support your development.

We focus on \"Train,\" \"Transfer,\" and \"Sustain\" – ensuring you master the concepts, gain on-the-job competence, and receive continuous evaluation and support. At IQVIA, we are always learning.

What You'Ll Be Doing:

Participate in a full-time, dedicated training program covering all aspects of clinical trial monitoring.
Learn and apply ICH-GCP guidelines, as well as Australian ethical and regulatory requirements.
Conduct site monitoring visits (under supervision), including selection, initiation, monitoring, and close-out.
Assist in managing study progress by tracking regulatory submissions, recruitment, and data completion.
Maintain accurate and organized study documentation, including Trial Master Files (TMF) and Investigator Site Files (ISF).
Collaborate with study teams and build strong working relationships with sites and colleagues.

What We'Re Looking For:

A bachelor’s degree in a health care or life-science field or equivalent experience
Prior experience in a clinical research setting, including roles such as In-house CRA, CTA, or CRC, is advantageous.
A basic understanding of ICH-GCP and the rules around clinical research in Australia.
Excellent English communication skills (written and verbal).
Proficiency in MS Office Suite.
Strong problem-solving, critical thinking, and time management skills.
Ability to build and maintain positive working relationships.

What to expect in the interview process:

You'll be asked to complete a pre-recorded video interview, online testing and if successful after this stage we ask you to attend an assessment interview in person
Video interviews and online assessment will take place between 25th September to the 15th October.
Candidates successful to the assessment day in office will be notified by 23rd October 2025.

Applications close Friday 3rd October 3pm

Interviews for New Zealand will be held at our Office on Thursday 30th October. This dates is fixed.
Start date with IQVIA is Monday 12th January 2026

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

","hiringOrganization":{"@type":"Organization","name":"IQVIA","sameAs":"https://www.iqvia.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Auckland, New Zealand","addressCountry":"New Zealand","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":12,"item":{"@type":"JobPosting","title":"Research Associate/Assistant","datePosted":"2025-09-24","description":"\n

Salary: Research Assistant: £33,002 - £34,610 per annum

Research Associate: £35,608 - £46.049 per annum

\n\n

Newcastle University is a great place to work, with excellent benefits. We have a generous holiday package; plus the opportunity to buy more, great pension schemes and a number of health and wellbeing initiatives to support you.

\n\n

Closing Date: 13 October 2025

\n\n

The Role

\n\n

We are seeking an ambitious post-doctoral researcher who will work with Dr Kavanagh in his Action Medical Research/LifeArc funded lab to develop new formulations of cysteamine for a rare disease, cystinosis. It's an exciting time to join our research group which currently has 4 members, 3 PhD students and a post-doctoral researcher and plans to hire 2 more PhD students by year-end.

\n\n

You will engage in cutting-edge research projects, collaborate with leading experts, and contribute to the advancement of knowledge in crystal engineering. We have links with The Newcastle upon Tyne Hospital groups and our central goal is to make a real difference for patients living with this condition. With a focus on high-impact publications and grant applications, the post-doc will have the opportunity to shape their own research agenda while working in a collaborative and supportive environment. This role is ideal for a self-driven and forward-thinking individual eager to make a significant impact in their academic career.

\n\n

This post is full time, fixed term for a period of one year.

\n\n

The start date for the post is 1 January 2026. For informal enquiries contact: oisin.kavanagh@newcastle.ac.uk
Find out more about the Faculty of Medical Sciences here: https://www.ncl.ac.uk/medical-sciences/
Find out more about our Research Institutes here: https://www.ncl.ac.uk/medical-sciences/research/institutes/

\n\n\n\n

Key Accountabilities

\n\n

Although working under the general guidance of an academic or Principal Investigator, you will contribute ideas, including enhancements to the technical or methodological aspects of your studies, thus providing substantial 'added value'
Develop and carry out the specified project using appropriate techniques and equipment as outlined in the personal requirements
Determine appropriate methodologies for research, with advice and support where required
Contribute to grant applications submitted by others and in time develop own research objectives and proposals for funding
Begin to write, with appropriate support, proposals for individual research funding or, where funders do not permit this, contribute to the writing of collective bids
Assess research findings for the need/scope for further investigations
Contribute to the writing up of their research for publication and dissemination, either through seminar and conference presentations or through publications
Present research findings, either at conferences or through publications in reputable outlets appropriate to the discipline
May be involved in the supervision, with guidance, of final year undergraduate research projects and in providing support to postgraduate research students or Research Assistants
Will need to work with the support staff and, on occasions, with undergraduate and postgraduate students, and interact intellectually with other academic members of the Institute
May contribute to events celebrating the public engagement of science/social sciences/humanities
Develop an awareness of University structures, policies and procedures and relevant issues in the higher education, research, social and political environment

The Person (Essential)

Knowledge, Skills and Experience

\n\n

Ability to work well as part of a team and rapidly acquire new skills
Detailed subject knowledge in either drug pharmacokinetics or drug behavior in solutions
Likelihood of advanced skills directly related to the research project (e.g. hands on experience of formulation design or crystal engineering)
High level of analytical and problem-solving capability
Ability to communicate complex information with clarity and to encourage the commitment of others
Experience of research with clear transferable skills and some experience or awareness of the research environment
Presentations at conferences and/or high-quality publications

\n\n

Attributes And Behaviour

\n\n

Essential

Diligent and reliable
Able to work flexibly to meet deadlines
Collaborative but also able to work independently
Resourceful but also willing to accept guidance

Qualifications

\n\n

Honours degree in chemistry, chemical engineering, pharmacy or pharmaceutical sciences (For Assistant level)
A PhD in relevant area (for Associate Level) or open to completing a PhD
Close to submission of PhD (for appointment at Assistant level which will be automatically upgraded to Associate once on the PhD passlist)

Newcastle University is a global University where everyone is treated with dignity and respect. As a University of Sanctuary, we aim to provide a welcoming place of safety for all, offering opportunities to people fleeing violence and persecution.

\n\n

We are committed to being a fully inclusive university which actively recruits, supports and retains colleagues from all sectors of society. We value diversity as well as celebrate, support and thrive on the contributions of all of our employees and the communities they represent. We are proud to be an equal opportunities employer and encourage applications from individuals who can complement our existing teams, we believe that success is built on having teams whose backgrounds and experiences reflect the diversity of our university and student population.

\n\n

At Newcastle University we hold a silver Athena Swan award in recognition of our good employment practices for the advancement of gender equality. We also hold a Race Equality Charter Bronze award in recognition of our work towards tackling race inequality in higher education REC. We are a Disability Confident employer and will offer an interview to disabled applicants who meet the essential criteria for the role as part of the offer and interview scheme.

\n\n

In addition, we are a member of the Euraxess initiative supporting researchers in Europe.

Requisition ID: 28646

","hiringOrganization":{"@type":"Organization","name":"Newcastle University","sameAs":"https://www.ncl.ac.uk"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Newcastle, GB","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":13,"item":{"@type":"JobPosting","title":"Research Associate (Science of Learning in Education Centre) [NIE]","datePosted":"2025-09-24","description":"

The National Institute of Education invites suitable applications for the position of Research Associate on a 12-month contract at the Science of Learning in Education Centre.

Project Title: DRivers, Enablers and pathways of Adolescent developMent in Singapore (DREAMS): The Singapore Longitudinal Cohort Study (SG-LCS) Phase 1 – Project 7

Project Introduction:

This study seeks primarily to understand (a) the nature of educational pathways made by students through secondary education, (b) the drivers of the decisions made about educational pathways through secondary education (especially self-identity and agency, school and career aspirations, and social and relational contexts), (c) the stability and change patterns of educational pathways as well as factors that may be associated with change. We expect the drivers of educational pathways to be interrelated, and (d) through retrospective investigation, the factors at early childhood and primary school that contribute to educational pathways. Furthermore, this study will allow focus on educational pathways of specific subgroups to understand the differential impact of educational pathways for (e) students with special educational needs (SEN) and (f) for students from financially disadvantaged environments.

Project 7 will focus on a specific subgroup of students from financially disadvantaged environments, investigating development and pathways of at-risk adolescents and other related inquiries.

Requirements

Essential

A Master’s Degree in Learning Sciences, Education, Psychology, Data Science, Educational Neuroscience or a related field; Applicants with a PhD may be considered for a Research Fellow position
Familiar with the Singapore education system (preferably with experience working with disadvantaged learners)
Familiar with major theories in learning sciences (e.g, adolescent development; individual differences; Educational neuroscience)
Proficient in using at least one statistical software package (e.g., SPSS, R, Stata, Mplus)
Experience in coordination and conduct of data collection and organization
Project management experience, including leading a research team, management of budget, and tracking of project progress
Possess strong interpersonal communication, writing and language skills
Able to work independently with minimal supervision.
Able to work cooperatively in both small (<3 pax) and large teams (>10 Pax)

Preferred

Proficient or knowledge with Machine Learning algorithms
Experience in conducting neuroimaging studies in educational contexts
Experience in working with databases.

Responsibilities

Liaise with stakeholders (E.g. participating schools/parents/teachers and other researchers involved in the project)
Planning, preparation, and implementation of data collection
Planning and analyses of data
Synthesising of information from research findings
Management of project-related matters (E.g. Budgeting, progress tracking)
Writing of reports, publications and preparation of presentation materials
Other tasks as assigned by the Principal Investigator / Co-PIs

Application

Applicants (external and internal) will apply via Workday. We regret that only shortlisted candidates will be notified.

Please include your name in your CV file name.

Closing Date

Closing date for advertisements will be set to 14 calendar days from date of posting.

Hiring Institution: NIE","hiringOrganization":{"@type":"Organization","name":"Nanyang Technological University","sameAs":"https://www.ntu.edu.sg/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"NTU Main Campus, Singapore","addressCountry":"Singapore","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":14,"item":{"@type":"JobPosting","title":"Securities Research Associate","datePosted":"2025-09-24","description":"

About This Role:

Wells Fargo is seeking a Securities Research Associate

In This Role, You Will:

Provide support in the editing and publishing functions within the Global Research and Economics Group in Wells Fargo Securities
Generate research packet products, post research documents to market data vendors, update and maintain mailing lists, and provide client access to web sites
Assign reports to Editors and Supervisory Analysts to ensure the most efficient use of resources
Maintain databases
Receive direction from leaders
Exercise independent judgment while developing the knowledge to understand function, policies, procedures, and compliance requirements
Collaborate and consult with peers, colleagues and managers to resolve issues and achieve goals
Assist on work streams that form key components of M&A buyside or sell-side deal execution and/or, corporate finance or capital market transactions across multiple sub-sectors in TMT
Assist in preparing pitchbook components including industry overviews, company profiles, management biographies, brokers’ outlook, share price performance, deal case studies, evolution of industry/peers valuation multiples, possible buyer/seller opportunities, amongst others
Assist in equity and debt capital raising (IPOs, follow-on offering, bond issuances etc.) and leveraged underwriting transactions
Work on comparable company analysis, precedent transaction analysis, buyer or target identification, company/M&A screening and sector updates and analyses
Work on financial analysis, industry benchmarking and valuation models
Develop an understanding of a sector’s key performance and valuation indicators and identify key industry and M&A trends and outlook impacting the sector
Develop excellent working knowledge of market databases e.g., FactSet, Refinitiv, Bloomberg, Dealogic, Merger Market, etc.
Interact with multiple stakeholders to achieve the desired goal

Required Qualifications:

2+ years of Securities Research experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education

Desired Qualifications:

MBA or master’s in finance from a premier education institute with 2+ years of relevant work experience with a good understanding of Industrials sub-sectors
Strong inclination towards building a career in Corporate Finance, Investment Banking or Capital Markets
Impeccable communication and interpersonal relationship skills with the ability to interact with senior professionals and key stakeholders
Good understanding of financial concepts and company valuation techniques
Strong logical, analytical skills and a systematic problem-solving approach
Ability to proficiently use Microsoft Office Applications – Power Point and Excel
Strong time management skills and ability to work under pressure and meet strict deadlines.
Attention to detail and ability to ensure high quality deliverables.
Ability to interact with integrity and a high level of professionalism with all levels of team members and management.
Results driven, accountable and ability to work with multiple priorities in a fast-paced and results-driven environment

Job Expectations:

Ability to proficiently use Microsoft Office Applications – Power Point and Excel
Knowledge of database tools – FactSet, Thomson one, Capital IQ, Factiva, and Bloomberg
Impeccable communication and interpersonal relationship skills with the ability to interact with senior professionals and key stakeholders
Strong time management skills and ability to work under pressure and meet strict deadlines
Attention to detail and ability to ensure high quality of deliverables
Ability to provide innovative ideas to efficiently execute the tasks
Ability to identify proactive ways to contribute to firm's goals & mission

Posting End Date:

29 Sep 2025

*Job posting may come down early due to volume of applicants.

We Value Equal Opportunity

Applicants With Disabilities

To request a medical accommodation during the application or interview process, visit Disability Inclusion at Wells Fargo.

Drug and Alcohol Policy

Wells Fargo maintains a drug free workplace. Please see our Drug and Alcohol Policy to learn more.

Wells Fargo Recruitment and Hiring Requirements:

Third-Party recordings are prohibited unless authorized by Wells Fargo.
Wells Fargo requires you to directly represent your own experiences during the recruiting and hiring process.

","hiringOrganization":{"@type":"Organization","name":"Wells Fargo","sameAs":"https://www.wellsfargo.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"110382-IND-HYDERABAD-INTL HYD WF CENTRE BLK 1B Twr-2, India","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":15,"item":{"@type":"JobPosting","title":"Securities Research Associate (ESG)","datePosted":"2025-09-24","description":"

Job Description

About This Role:

Wells Fargo is seeking a Securities Research Associate

In This Role, You Will:

Provide support in the editing and publishing functions within the Global Research and Economics Group in Wells Fargo Securities
Generate research packet products, post research documents to market data vendors, update and maintain mailing lists, and provide client access to web sites
Assign reports to Editors and Supervisory Analysts to ensure the most efficient use of resources
Maintain databases
Receive direction from leaders
Exercise independent judgment while developing the knowledge to understand function, policies, procedures, and compliance requirements
Collaborate and consult with peers, colleagues and managers to resolve issues and achieve goals

Required Qualifications:

2+ years of Securities Research experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education

Desired Qualifications:

Investment banking experience of 2+ years post MBA / CA
Prior Environmental Social Governance (ESG) experience, analytics and sustainable finance experience is preferred
Corporate & Investment Banking delivers a comprehensive suite of capital markets, banking, and financial products and services. A trusted partner to our clients, we provide corporate and transactional banking; commercial real estate lending and servicing; investment banking; equity; and fixed income solutions including sales, trading, and research capabilities to corporate, commercial real estate, government, and institutional clients across the globe.
The Sustainable Finance Advisory group within Corporate and Investment Banking is seeking an Associate to join its Bangalore office.
The Analyst will be responsible for supporting the development of our ESG strategy for both external client engagement and internal projects that help us meet our climate and sustainable finance goals, including but not limited to, the following activities:
Partner with senior bankers to create client-and situation-specific materials on ESG considerations across lending, debt capital markets, equity capital markets, advisory engagements, risk management and liquidity
Research competitive dynamics, market developments, investor trends, and industry best practices.
Help develop segment specific ESG analysis to support strategic client dialogue, including investor and reporting trends, third-party methodologies and industry standards.
Support the development of innovative products and solutions that address the evolving ESG-related needs of clients and investors.
Provide support through research and the creation of presentation materials for the development of CIB’s efforts to meet our Company’s Net Zero by 2050 and $500B in sustainable finance by 2030.
Collaborate with a wide range of internal stakeholders to support this broad, growing and dynamic aspect of banking
Expected to work on assigned tasks independently with guidance on the more complex transactions
Employees support our focus on building strong customer relationships balanced with a strong risk mitigating and compliance-driven culture which firmly establishes those disciplines as critical to the success of our customers and company. They are accountable for execution of all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which include effectively following and adhering to applicable Wells Fargo policies and procedures, appropriately fulfilling risk and compliance obligations, timely and effective escalation and remediation of issues, and making sound risk decisions. There is emphasis on proactive monitoring, governance, risk identification and escalation, as well as making sound risk decisions commensurate with the business unit’s risk appetite and all risk and compliance program requirements.
Investment banking experience of 2-4 years post MBA / CA
Prior Environmental Social Governance (ESG) experience, analytics and sustainable finance experience is preferred

Posting End Date:

30 Sep 2025

*Job posting may come down early due to volume of applicants.

We Value Equal Opportunity

Applicants With Disabilities

To request a medical accommodation during the application or interview process, visit Disability Inclusion at Wells Fargo.

Drug and Alcohol Policy

Wells Fargo maintains a drug free workplace. Please see our Drug and Alcohol Policy to learn more.

Wells Fargo Recruitment and Hiring Requirements:

Third-Party recordings are prohibited unless authorized by Wells Fargo.
Wells Fargo requires you to directly represent your own experiences during the recruiting and hiring process.

","hiringOrganization":{"@type":"Organization","name":"Wells Fargo","sameAs":"https://www.wellsfargo.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"111442-IND-BENGALURU-INTL BLR BLK B3 PETUNIA, India","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":16,"item":{"@type":"JobPosting","title":"Research Associate (Science of Learning in Education Centre) [NIE]","datePosted":"2025-09-24","description":"

The National Institute of Education invites suitable applications for the position of Research Associate on a 12-month contract at the Science of Learning in Education Centr e.

Project Title:

PROSPER: Promoting Neuroprotective Out-of-classroom Playful Learning Interventions for Cognitive and Socio-Emotional Mathematical Competence of Pre-schoolers

Project Introduction:

We are seeking a highly motivated and skilled Research Associate/Fellow to join our interdisciplinary team working on a cutting-edge research project titled \" PROSPER: Promoting Neuroprotective Out-of-classroom Playful Learning Interventions for Cognitive and Socio-Emotional Mathematical Competence of Pre-schoolers.\" This project aims to implement neuroprotective playful learning interventions for cognitive and socioemotional mathematical competency development. The successful candidate will play a crucial role in designing, implementing, and evaluating these interventions to advance our understanding of how playful learning interventions can support mathematics learning and well-being.

Requirements:

A Masters or equivalent degree in education, psychology, neuroscience, learning environments or a related field. (Candidates with a PhD may be considered for a Research Fellow position instead)
Strong background in research methodology, with experience in designing and conducting empirical studies.
Expertise in learning environments, development, and evaluation.
Familiarity with design principles and planning tools that are used in creating learning environments.
Familiarity with digital biomarkers, data analytics, and machine learning techniques.
Proficiency in statistical analysis and familiarity with software like SPSS, R, or Python
Excellent communication skills, with the ability to collaborate effectively with interdisciplinary teams and communicate research findings to diverse audiences.
Prior experience working with young children and families is preferred but not required.

Responsibilities:

Conducting comprehensive literature reviews on topics related to neuroprotection, learning environments, and educational psychology.
Collect and analyze data using digital biomarkers and other relevant measures for pre-school learners.
Management of multiples aspects of the research project, including project management, liaising with stakeholders, data collection, and analysis.
Disseminate research findings through academic publications, research presentations, and outreach activities.
Perform other tasks as assigned by the Principal Investigator and Co-Principal Investigators

Application

Applicants (external and internal) will apply via Workday. We regret that only shortlisted candidates will be notified.

Closing Date

Closing date for advertisements will be set to 14 calendar days from date of posting.

Hiring Institution: NIE","hiringOrganization":{"@type":"Organization","name":"Nanyang Technological University","sameAs":"https://www.ntu.edu.sg/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"NTU Main Campus, Singapore","addressCountry":"Singapore","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":17,"item":{"@type":"JobPosting","title":"Research Associate - Plant Physiology/Biochemistry","datePosted":"2025-09-23","description":"

Kindly be advised that we are handling the recruitment for this position internally and are not partnering with external recruiters.

We are a Biology Company

Plantible, backed by Astanor Ventures, Lerer Hippeau, Piva Capital, Kellogg’s, and Vectr Ventures, is a vertically integrated biology company that is unlocking the power in plants in service of people & planet. Our mission is to create solutions that empower customers to make sustainable and regenerative choices without compromising on quality. We are beginning with the food industry. Please visit our website to learn more about our mission and continued success: https://www.plantiblefoods.com/

How You Will Contribute:

We are seeking a passionate and mission-driven Research Associate (RA) Plant Physiologist/Biochemist with theoretical knowledge in plant molecular biology and biochemistry and has a good understanding of plant ecophysiology with hands-on lab experience with various lab operations like PCR, Western blotting, gas exchange measurements, and spectrophotometric assays. This individual will develop and execute lab and field experiments to improve our understanding of duckweed physiology using thorough data analysis and working collaboratively with our team of RA’s, Scientists, and Operators. The individual will have the opportunity to make an immediate and sustainable impact on the development of the company.

What you will be working on:

Design, execute, and analyze lab and field experiments to improve the quality and quantity of our plant protein and to increase biomass productivity.
Use SDS-PAGE, Western blotting, and enzyme activity assays to measure the quality and quantity of target proteins present in duckweed.
Measure physiological processes of duckweed.
Use molecular biology techniques to genotype duckweed strains.
Determine abiotic and biotic effects on duckweed growth.
Use microscopy to characterize duckweed anatomy.

What You Bring To Plantible:

BS in Biological Sciences/Plant Physiology with 2+ years of experience in an industry setting or MS in Plant Biology/Plant Physiology with up to 1+ years of experience in an industry setting.
Previous lab and field experience with growing plants, measuring physiological parameters, and performing basic molecular biology and biochemistry techniques.
An understanding of biotic and abiotic factors that affect biomass productivity and knowledge of plant metabolic processes.
Excellent verbal and written communication and presentation skills.
Excellent time management and organizational skills.
Ability to thrive in a startup lab environment.
Ability to learn quickly, solve complex problems and have excellent data analysis skills.
Being a self-starter and able to respond creatively and simply to continuous change and steady growth environment.
Team player spirit and an open mind to contribute towards company goals.
Willingness to travel for 25% and possibly up to, but no more than, 50% of the year for work.
Thrive in a fast-paced environment where the primary focus is on simplification, stabilization and optimization.

Choose Plantible Foods

Joining Plantible means contributing to a sustainable future for all. We are a venture backed startup that is both spreading happiness amongst our employees and to current and future generations. We believe diversity creates uniqueness. Our team is composed of highly talented people with different interests and hobbies, which makes for a rich working environment.

At Plantible we are continually working on our offerings to foster the best team. Check it out!

Competitive health and wellness benefits
Medical, Dental and Vision Insurance
Discretionary Unlimited PTO Program
Paid Holidays
401k Program
Career Stipend
Career development and growth opportunities
Working in a rapidly growing, flexible and entrepreneurial environment
Team building and company-wide events
Financial support with your relocation, if necessary, ensuring a smooth transition

Plantible Foods is an equal employment opportunity employer. Candidates are considered for employment without regard to race, creed, color, national origin, age, sex, religion, ancestry, veteran status, marital status, gender identity, sexual orientation, national origin, liability for military service, or any other characteristic protected by applicable federal, state, or local law. If you are interested in learning the status of your application, please note you will be contacted directly by the appropriate human resources contact person if you are selected for further consideration. Plantible Foods reserves the right to defer or close a vacancy at any time.

If you feel your skill set does not meet all listed qualifications for the role, we still encourage you to apply. As we continue to grow our company, we are seeking a range of candidates and would gladly consider you for other current or upcoming roles that may be a fit!

","hiringOrganization":{"@type":"Organization","name":"Plantible Foods","sameAs":"https://www.plantiblefoods.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Vista, CA","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":18,"item":{"@type":"JobPosting","title":"CRM Coordinator – Global CRM Support","datePosted":"2025-09-23","description":"

Description

About Mcm

MCM (Modern Creation München) is a luxury lifestyle goods and fashion house founded in 1976 with an attitude defined by cultural Zeitgeist and German heritage. With a focus on functional innovation and a bold, aspirational spirit, MCM connects with a global audience across music, art, travel, and technology. Distributed in over 650 stores worldwide, MCM is driven to revolutionize classic design with futuristic materials for the 21st Century Global Nomad.

Position Overview

The CRM Coordinator will play a pivotal role in supporting MCM’s global CRM initiatives with a focus on North America, working closely with cross-functional and global teams. This hands-on role supports daily CRM operations including customer segmentation, maintaining data accuracy, and providing clienteling application assistance, while helping to build performance dashboards and track KPIs such as retention, reactivation, and campaign ROI. The CRM Coordinator will assist in executing targeted campaigns tied to product launches and seasonal promotions, partner with stores and customer service to incorporate client feedback, and help test and implement new integrations, tools, and processes. The ideal candidate thrives in a fast-paced, multicultural environment and is passionate about enhancing the client experience through data-driven strategies, cross-functional collaboration, and operational excellence.

Key Responsibilities

Assist in managing day-to-day CRM operations, including customer segmentation, clienteling application support, retail store assistance, and database analysis.
Maintain high standards of data quality and accuracy across CRM platforms, clienteling apps, and related systems.
Build, update, and maintain CRM dashboards and performance reports to track KPIs such as retention, reactivation, and campaign ROI.
Collaborate with cross-functional teams (e.g., product, analytics, merchandising, retail) to support targeted CRM campaigns aligned with product launches, seasonal promotions, and business objectives.
Partner with global teams to ensure consistency, alignment with brand objectives, and achievement of strong CRM KPIs.
Lead reporting and analytics, identifying opportunities for process improvements and optimization in sales workflows.
Assist with vendor communication and ensure timely resolution of CRM or application-related issues.
Conduct testing for new integrations, campaigns, and platform enhancements, providing hands-on system support for CRM and clienteling tools.
Partner with stores and customer service teams to gather and integrate customer feedback into CRM strategies.
Monitor CRM adoption rates, recommending strategies to drive engagement and operational efficiency.
Coordinating initiatives across multiple NCSA markets with varying time zones and business needs
Exposure to global luxury retail CRM strategies and multi-market campaign execution.
Hands-on involvement in both operational and creative aspects of CRM, with opportunities to influence client engagement strategies.

Requirements

Job Requirements:

Minimum 2 years’ experience in CRM, marketing operations, or related fields.
Hands-on experience with Salesforce CRM, Excel, PowerPoint, and Proximity (or similar clienteling tools).
Strong attention to detail with excellent data management skills.
Advanced Excel and PowerPoint skills with the ability to create insightful, visually compelling reports and dashboards.
Data-driven mindset with the ability to analyze customer behavior, evaluate campaign performance, and drive client retention strategies.
Exceptional organizational skills with the ability to manage multiple priorities and deadlines.
Strong interpersonal skills for working effectively across regions, time zones, and business functions.
Quick learner who adapts well to change and thrives in a collaborative, high-energy team culture.
Previous experience in retail or luxury fashion preferred.

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Position Summary

The Postdoctoral Fellow will oversee a research project to test a novel therapeutic in a rat model of AD. The project involves expertise in animal models of AD/neurodegenerative disease, animal surgeries and treatments, behavioral assessments, and postmortem pathological analyses including histological, biochemical, and functional genomic/proteomic techniques. The Fellow will also be involved in other lab projects including 1) human tissue-based studies on mechanisms of mild cognitive impairment (MCI) and AD, and 2) additional in vivo studies of vascular contributions to MCI and AD. Duties will include helping in the day-to-day operations of the lab, collaborative experimental design, conducting independent research, data analysis, presenting data at conferences, and writing manuscripts for publication in peer-reviewed journals. The applicant will also gain exposure in mentoring graduate students and other professional development opportunities to promote an independent career. This position is in Grand Rapids, MI.

Equal Employment Opportunity Statement

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, age, disability or protected veteran status.

Required Degree

Doctorate -Alzheimer's disease, Dementia, Neurodegeneration

Minimum Requirements

The position requires a doctoral degree in neuroscience (or a related program) focused on AD research including animal models of disease. Individual should be familiar with common biological laboratory research techniques and have a basic understanding of biochemistry, molecular biology, cell biology and physiology. Applicants should be able to demonstrate his or her experience with conducting research studies independently, fundamental statistical analysis, and the preparation of results for publication as a scientific manuscript. At least one first author paper in a peer-reviewed journal is expected.

Desired Qualifications

Experience with some or all of the following techniques is desired: Rodent surgeries, treatments, and behavioral analysis; human and rodent tissue processing, immunohistochemistry, and microscopic analysis; stereologic procedures or machine-learning quantitative analysis; RNA sequencing and/or proteomics; advanced molecular biology and biochemical techniques such as cloning, gene regulation, and protein analysis; cell culture modeling; and statistical analysis including familiarity with R or similar programs. Highly competitive applicants will have multiple authorships including at least one first-author manuscript in a peer-reviewed journal.

Required Application Materials

Curriculum Vitae, Names of 3 references, 1-2 page statement highlighting past accomplishments and future goals.

Review Of Applications Begins On

10/01/2025

Summary Of Health Risks

Work with animals or unfixed animal tissue

Website

http://translationalscience.msu.edu/

Msu Statement

Michigan State University has been advancing the common good with uncommon will for more than 160 years. One of the top research universities in the world, MSU pushes the boundaries of discovery and forges enduring partnerships to solve the most pressing global challenges while providing life-changing opportunities to a diverse and inclusive academic community through more than 200 programs of study in 17 degree-granting colleges.

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Company Description

About M3: A Japanese global leader in the provision of ground-breaking and innovative technological and research solutions to the healthcare industry. The M3 Group operates in the US, Asia, and Europe with over 5.8 million physician members globally via its physician websites which include mdlinx.com, m3.com, research.m3.com, Doctors.net.uk, medigate.net, and medlive.cn. M3 Inc. is a publicly traded company on the Tokyo Stock Exchange (jp:2413, NIKKEI 225) with subsidiaries in major markets including the US, UK, Japan, South Korea, and China, and in 2020 was ranked in Forbes’ Global 2000 list. The M3 Group provides services to healthcare and the life science industry. In addition to market research, these services include medical education, ethical drug promotion, clinical development, job recruitment, and clinic appointment services. M3 has offices in Japan, UK, France, Germany, Brazil, Sweden, China, USA, and South Korea, as well as India.

About The Business Division:

This role is part of QQFS, a Gothenburg based fieldwork agency and a wholly owned subsidiary of M3 Inc. QQFS is a leading provider of data-collection services for the pharmaceutical and healthcare industry. We specialize in conducting both qualitative and quantitative market research in The Nordics and Benelux regions, in addition to Austria and Switzerland.

Job Description

Essential Duties And Responsibilities:

Including, but not limited to the following:

Project Recruitment

Ensure that recruitment tasks assigned for projects in Scandinavia region and any other QQFS assigned markets are fully executed
Reach out to M3 Global Research panelists via phone and carry out cold calling to recruit respondents on allocated projects
Scheduling interviews
Proactively plan, organize and implement panel recruitment solutions on allocated projects, aiming to maximize internal resources, reduce outsource cost and ensure successful project delivery
Provide updates in the given format and timings to the project management team on the work done for projects, progress, results and action plans to deliver the allocated studies within the provided timelines and specs
Flag to the senior manager projects of concern, when recruitment progress is off track and it is likely to require partners
Ensure that outsource targets for allocated markets are achieved

Panel building and engagement

Ensure that monthly registrations targets are met for Scandinavia region
and any other QQFS assigned markets are fully executed
Execute the allocated panel building initiatives in Scandinavia region
and any other QQFS assigned markets are fully executed
Call new registrants to confirm and update email addresses
Call users to reactivate their accounts
Work across multiple systems to investigate, troubleshoot and handle inquiries and complaints, provide appropriate solutions and alternatives, and follow up to ensure resolution
Work with the Project Management team to resolve project specific issues for members/respondents
Ensure that respondent inquiries are handled according to company policy regarding outcomes and time to resolution
Provide input on and assist with updating communication procedures, guidelines, and enhancements to the Support Ticket System
Build and maintain strong relationships with the panel members through timely and professional communication across multiple channels
Provide high quality support to M3 Global Research members via telephone and email/support ticket communication
Work with other members of the global Panel team, report and resolve potential issues with internal and external systems and processes
Investigate fraud respondents and take action based on M3 data quality procedures
Complete the verification process for newly registered members
Complete link testing for online Market Research projects and overlays for qualitative online screeners

Qualifications

Knowledge, Skills, Abilities:

Fluency in one of the Scandinavian languages (Danish, Swedish, Norwegian) and English
Exhibit clear and effective communication both verbally and written with diverse audiences
Proficient PC skills including Microsoft Office tools, Internet, Social Media, e-mails and tools required within assigned responsibilities
Detail oriented with excellent analytical and investigative skills
Ability to ask probing questions, respond effectively and accurately, and ensure audiences feel supported.

Additional Information

#Li-Lc1\n#Li-Remote

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Company Description

About The Business Division:

Job Description

Essential Duties And Responsibilities:

Including, but not limited to the following:

Project Recruitment

Ensure that recruitment tasks assigned for projects in Scandinavia region and any other QQFS assigned markets are fully executed
Reach out to M3 Global Research panelists via phone and carry out cold calling to recruit respondents on allocated projects
Scheduling interviews
Proactively plan, organize and implement panel recruitment solutions on allocated projects, aiming to maximize internal resources, reduce outsource cost and ensure successful project delivery
Provide updates in the given format and timings to the project management team on the work done for projects, progress, results and action plans to deliver the allocated studies within the provided timelines and specs
Flag to the senior manager projects of concern, when recruitment progress is off track and it is likely to require partners
Ensure that outsource targets for allocated markets are achieved

Panel building and engagement

Ensure that monthly registrations targets are met for Scandinavia region
and any other QQFS assigned markets are fully executed
Execute the allocated panel building initiatives in Scandinavia region
and any other QQFS assigned markets are fully executed
Call new registrants to confirm and update email addresses
Call users to reactivate their accounts
Work across multiple systems to investigate, troubleshoot and handle inquiries and complaints, provide appropriate solutions and alternatives, and follow up to ensure resolution
Work with the Project Management team to resolve project specific issues for members/respondents
Ensure that respondent inquiries are handled according to company policy regarding outcomes and time to resolution
Provide input on and assist with updating communication procedures, guidelines, and enhancements to the Support Ticket System
Build and maintain strong relationships with the panel members through timely and professional communication across multiple channels
Provide high quality support to M3 Global Research members via telephone and email/support ticket communication
Work with other members of the global Panel team, report and resolve potential issues with internal and external systems and processes
Investigate fraud respondents and take action based on M3 data quality procedures
Complete the verification process for newly registered members
Complete link testing for online Market Research projects and overlays for qualitative online screeners

Qualifications

Knowledge, Skills, Abilities:

Fluency in one of the Scandinavian languages (Danish, Swedish, Norwegian) and English
Exhibit clear and effective communication both verbally and written with diverse audiences
Proficient PC skills including Microsoft Office tools, Internet, Social Media, e-mails and tools required within assigned responsibilities
Detail oriented with excellent analytical and investigative skills
Ability to ask probing questions, respond effectively and accurately, and ensure audiences feel supported.

Additional Information

#Li-Lc1\n#Li-Remote

","hiringOrganization":{"@type":"Organization","name":"M3 USA","sameAs":"https://usa.m3.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Gothenburg, Västra Götaland County, Sweden","addressCountry":"Sweden","addressRegion":"Europe"}}}},{"@type":"ListItem","position":22,"item":{"@type":"JobPosting","title":"Clinical Research Associate II","datePosted":"2025-09-23","description":"

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You Will:

Act as the main line of communication between the project team, sponsor, and the site
Build and maintain a good relationship with the site staff involved in the study conduct
Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits
Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at site level
Ensure accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations
Perform source data verification and follows up on data queries at site level; review and manage study risks on a site level
Ensure proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on sites
Review essential study documents and reconcile study Investigator Site File (ISF) / TMF at site level
Ensures quality (data integrity and compliance) at site level
Conduct site audit preparation visits and resolve site audit findings
Participate in study site audits and client onsite visits, as required
Ensure the flow of documents and study supplies between the project team, site and the Central/ Regional Laboratory/ Central Reviewer/ Warehouse
Conduct project-specific training of site investigators
Support preparation of Investigator newsletters
Assist Site Management Associates in maintaining study-specific and corporate tracking systems at site level
Support preparation of draft regulatory and ethics committee submission packages
Support collection of IP-RED packages at site/country level
Facilitate review and reconciliation of the study TMF on country and site levels

Qualifications

College/University degree in Life Sciences or an equivalent combination of education, training & experience
Located in Central or West Coast preferred*
2+ years of independent on-site monitoring experience required
Experience in all types of monitoring visits, in phases I-III
Experience in Oncology mandatory & GI preferred and/or radio-pharm experience preferred.
Full working proficiency in English
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel up to 75%
Valid driver’s license (if applicable)

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.

For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

","hiringOrganization":{"@type":"Organization","name":"PSI CRO","sameAs":"https://www.psi-cro.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Remote, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":23,"item":{"@type":"JobPosting","title":"Postdoctoral Research Associate - Chemistry | Catalysis Science (Heterogeneous)","datePosted":"2025-09-23","description":"

Title: Postdoctoral Research Associate - Chemistry | Catalysis Science (Heterogeneous)

Employee Classification: Postdoctoral Research Assoc

Campus: University of North Texas

Division: UNT-Provost

SubDivision-Department: UNT-College of Science

Department: UNT-Chemistry-121200

Job Location: Denton

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

Salary: Compensation is competitive and commensurate with the candidate’s qualifications, experience, and discipline, in accordance with university guidelines and available funding.

FTE: 1.00
Retirement Eligibility: ORP Eligible
About Us - Values Overview

\n\n\n\n\n\n\nWelcome to the University of North Texas System. The UNT System includes the University of North Texas in Denton and Frisco, the University of North Texas at Dallas and UNT Dallas College of Law, and the University of North Texas Health Science Center at Fort Worth. We are the only university system based exclusively in the robust Dallas-Fort Worth region. We are growing with the North Texas region, employing more than 14,000 employees, educating a record 49,000+ students across our system, and awarding nearly 12,000 degrees each year.\n \nWe are one team comprised of individuals who are committed to excellence, curiosity and innovation. We are transforming lives and creating economic opportunity through education. We champion a people-first values-based culture where We Care about each other and those we serve. We believe that we are Better Together because we foster an environment of respect, belonging, and access for all. We demonstrate Courageous Integrity through setting exceptional standards and acting in the best interest of our communities. We are encouraged to Be Curious about opportunities for learning, creating, discovering, and innovating, and are encouraged to learn from failure. Show Your Fire by joining our team and exhibiting your passion and pride in your work as part of our UNT System team.\n \nLearn more about the UNT System and how we live our values at www.UNTSystem.edu.\n \n\n\n\n\n

Department Summary

The Department of Chemistry provides opportunities for undergraduate and graduate students interested in cutting-edge technology and research. We allow students to pursue their scientific creativity with guidance from leading chemistry faculty.

UNT has a highly diverse campus with a wide range of languages spoken in addition to English. We welcome candidates who have experience with HSI/MSIs and/or who speak Spanish, Vietnamese, American Sign Language, Chinese (Cantonese, Mandarin and other variations), Arabic, Tagalog, Farsi, French, or/and Yoruba.

\n\n\n\n\n

Position Overview

The primary purpose of this position is to conduct research in the field of Catalysis Science (Heterogeneous) in the PI, Dr. Linxiao Chen’s group at UNT. The postdoctoral scientist will plan, execute, and analyze experiments involving the synthesis, spectroscopic characterization of heterogeneous catalysts, and catalytic reaction kinetics. The postdoctoral scientist will also instruct and oversee graduate and undergraduate students involved in the research, and contribute to writing proposals and papers.

This position will provide abundant freedom in research directions and topics, under the umbrella of Heterogeneous Catalysis. The postdoctoral scientist is encouraged to propose and pursue original, novel ideas in thermal, photo-, and/or electro-catalysis that are of common interest with the PI. Research topics of interdisciplinary, fundamental, and collaborative nature is especially encouraged. In addition to the ample resources at UNT, Chen Group can provide broad collaboration opportunities, and frequent access state-of-the-art capabilities at DOE’s national laboratories for catalysis studies, such as synchrotron and in-situ electron microscopy.

\n\n\n\n\n

Minimum Qualifications

• Ph.D. in a field related to Heterogeneous Catalysis (e.g., Chemistry, Chemical Engineering, Physics, Materials Science)
• Research experience in Heterogeneous Catalysis (thermal, photo-, or electro-)
• Ability to conduct doctoral-thesis-level research independently

Employees in this job may be responsible for conducting research on, working on, or having the ability to access critical organizational infrastructure and they must be able to maintain the security and integrity of the infrastructure related to this role.

\n\n\n\n\n

Preferred Qualifications

• Strong interest in the fundamental science of heterogeneous catalysis
• Interest in learning and exploring new areas/techniques out of comfortable zone
• Expertise in at least one of the three areas: 1) precise synthesis of well-defined catalytic materials; 2) flow-reactor kinetic analysis; 3) advanced in-situ spectroscopy
• Familiarity and interest in spectroscopic techniques for catalyst characterization, particularly synchrotron techniques
• Experience in collaborative research environment
• Strong communication skills

\n\n\n\n\n

Required License/Registration/Certifications

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

Job Duties

plan and execute experiments and data analysis
contribute to writing proposals and papers
contribute to training and supervision of graduate and undergraduate students

\n\n\n\n\n

Work Schedule

varies based on assignment

\n\n\n\n\n

Driving University Vehicle

No

\n\n\n\n\n

Security Sensitive

This is a Security Sensitive Position.

\n\n\n\n\n

Special Instructions

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

Benefits

For information regarding our Benefits, click here.

\n\n\n\n\n

Eeo Statement

The University of North Texas System is firmly committed to equal opportunity and does not permit -- and takes actions to prevent -- discrimination, harassment (including sexual violence, domestic violence, dating violence and stalking) and retaliation on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, or veteran status in its application, employment practices and facilities; nor permits race, color, national origin, religion, age, disability, veteran status, or sex discrimination and harassment in its admissions processes, and educational programs and activities, facilities and employment practices. The University of North Texas System promptly investigates complaints of discrimination, harassment and related retaliation and takes remedial action when appropriate. The University of North Texas System also takes actions to prevent retaliation against individuals who oppose any form of harassment or discriminatory practice, file a charge or report, or testify, assist or participate in an investigative proceeding or hearing.

\n\n\n\n\n","hiringOrganization":{"@type":"Organization","name":"University of North Texas System","sameAs":"https://www.untsystem.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Denton","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":24,"item":{"@type":"JobPosting","title":"Senior Clinical Research Associate I","datePosted":"2025-09-23","description":"

Company Description

PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Senior CRA I, 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.
\nYou will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.

Office-Based / Home-Based

Your Responsibilities Will Include:

Conducting and reporting all types of onsite monitoring visits
Driving the study startup phase (if applicable)
Performing CRF reviews, source document verification and query resolution
Be responsible for site communication and management
Supervising study activities, timelines, and schedules for each site
Acting as a point of contact for in-house support services and vendors
Supporting quality control, such as compliance monitoring and reports review
Participating in feasibility research
Supporting the regulatory team in preparing documents for study submissions and regulatory approval

Qualifications

BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
Independent on-site monitoring experience in the Czech Republic, ideally on multiple projects at a time
Demonstrable experience in all types of monitoring visits in Phase II and/or III
Strong written and verbal communication skills
Full professional proficiency in Czech and English
Experience supporting Oncology studies is beneficial, but not essential
Intermediate to Advanced knowledge of MS Office
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills are essential
As you will be monitoring multiple sites, you must have a full and clean driver's license, and the ability to travel.

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.

","hiringOrganization":{"@type":"Organization","name":"PSI CRO","sameAs":"https://www.psi-cro.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Prague, Prague, Czechia","addressCountry":"Czechia","addressRegion":"Europe"}}}},{"@type":"ListItem","position":25,"item":{"@type":"JobPosting","title":"Research Associate, CRM Support","datePosted":"2025-09-23","description":"Research Associate, CRM Support - (250002R4)

Entity: The Aga Khan University Medical College

Location: Karachi, Pakistan

Introduction:
The Aga Khan University Medical College (MC) was established in 1983, as a part of the Aga Khan University’s Faculty of Health Sciences in Karachi, Pakistan. It works closely with the School of Nursing and Midwifery and the University Hospital to produce excellence in educational programs and medical practice.

The Centre for Regenerative Medicine and Stem Cell Research (CRM) is a part of the MC. The Aga Khan University (AKU) has partnered with the University of California, San Francisco (UCSF) - an internationally renowned Center for Regenerative Medicine and Stem Cell Research, in developing and evolving The Aga Khan University Centre for Regenerative Medicine and Stem Cell Research (CRM). The Centre has a state-of-the-art facility for multi-disciplinary researchers to undertake cutting-edge research on stem cell and regenerative medicine. CRM nurtures young researchers (scientists and clinical scientists) in an environment that fosters learning and innovation.

As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopting appropriate standards for safeguarding and promoting a respectful relationship with and between the diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment.

CRM is inviting applications for the position of Research Associate, Centre for Regenerative Medicine and Stem Cell Research (CRM).

Responsibilities:

Reporting directly to the Principal Investigator (PI), the incumbent will be responsible for:

conducting wet lab supervised research related to the project
conducting daily, weekly, and monthly inventory of consumables/reagents required for the team
keeping record of procurement, follow-ups, receipts of supplies etc.
participating in weekly project meetings, journal clubs, research in progress meetings, and delivering presentations as directed by the assigned faculty
assisting with writing manuscripts, annual reports, and others.

Requirements:

You Should Have:

minimal master’s degree
one year of experience in the field of biological science research (Fresh candidates can also apply)
strong organizational skills with ability to handle multiple tasks
competent in computer usage with command over Microsoft Excel, PowerPoint, and Word
sound communication skills: fluent in English speaking and writing
strong interpersonal and mediation skills.

Comprehensive employment reference checks will be conducted.

Only shortlisted candidates will be contacted.

Primary Location

: Pakistan

Organisation

: Aga Khan Hospital & Medical College

Employee Status

: Contractual

Job Type

: Standard

Job Posting

: 23/09/2025, 3:41:37 AM

Closing Date

: 07/10/2025, 6:59:00 PM","hiringOrganization":{"@type":"Organization","name":"Aga Khan University","sameAs":"https://www.aku.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pakistan","addressCountry":"Pakistan","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":26,"item":{"@type":"JobPosting","title":"Research Associate, CRM Support","datePosted":"2025-09-23","description":"Research Associate, CRM Support - (250002R9)

Entity: The Aga Khan University Medical College

Location: Karachi, Pakistan

CRM is inviting applications for the position of Research Associate, Centre for Regenerative Medicine and Stem Cell Research (CRM).

Responsibilities

Reporting to the Assistant Manager and Manager CRM Lab and Core facility, and the Director Research & Teaching Laboratories, the incumbent will be responsible for:

independently operating one or more core facilities, including Pathology, FACS/Flow Cytometry
following (where applicable) and/or develop Standard Operating Procedures (SOPs) related to the core facilities.
undertaking regular weekly maintenance of all the equipment in the core lab and assisting in quarterly preventive maintenance with Bio-Medical Engineering Department
conducting daily, weekly, and monthly inventory of consumables required for the smooth operation of core/s
assisting and advising faculty and researchers in designing their projects
logging and recording all the communications, transactions, and maintenance schedules systematically and orderly
maintain database of all projects
preparing periodic and annual budgets for the profitable operation of the core including cost recovery and projections for a successful business plan
developing and maintaining inventory of all projects, equipment, consumables, service record, SOPs,manuals etc.
presenting to the faculty and CRM researchers the utility of the facility, challenges, and solutions
conducting training workshops and seminars in concepts, methodology, and operations of core facility
serving as backup to operate other research cores as and when needed.

Requirements:

You Should Have:

minimal master’s degree
one year of experience in the field of biological science research (Fresh candidates can also apply)
experience in operating one or more core facilities
strong organizational skills with the ability to handle multiple tasks assigned by the Assistant Manager and Manager, CRM Lab
excellent in computer usage with command over Microsoft Excel, PowerPoint, and Word
strong interpersonal and communication skills (spoken and written).

Comprehensive employment reference checks will be conducted.

Only shortlisted candidates will be contacted.

Primary Location

: Pakistan

Organisation

: Aga Khan Hospital & Medical College

Employee Status

: Contractual

Job Type

: Standard

Job Posting

: 23/09/2025, 3:57:48 AM

Closing Date

: 07/10/2025, 6:59:00 PM","hiringOrganization":{"@type":"Organization","name":"Aga Khan University","sameAs":"https://www.aku.edu/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pakistan","addressCountry":"Pakistan","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":27,"item":{"@type":"JobPosting","title":"Clinical/HC Research Associate - ICTS - Clinical Research Unit","datePosted":"2025-09-23","description":"Clinical/HC Research Associate - ICTS - Clinical Research Unit - (25005381)

Description

The clinical research nurse is at the front line of medical innovation, helping research teams test the lates treatments and clinical assessments. Our highly trained and skilled nurses are the front-line staff involved in administering these new compounds to research participants via multiple routes, including, but not limited to, IV, IM, SC, PO, Topical, Inhalation etc. Then monitor the research participants health status around the clock as per the trial protocol to ensure their safety and wellbeing.

The clinical research nurse for the Institute for Clinical and Translational Science (ICTS) will be an integral member of the team who specializes in delivering professional nursing care focused on maintaining balance between safety of the research participant and the fidelity to the research protocol interfacing with administration, clinical nursing staff, research staff, physicians, patients and families.

Duties to include but not limited to:

Provides direct nursing care including infusions, medication administration all routes and assessments in relation to the research protocol to attain expected measurable outcomes.
Provides nursing care to acute and complex patient populations and utilizes appropriate professional judgment and critical decision making in planning and providing care.
Collaborates with nursing, medical staff and research professionals in the review of clinical research protocols in relationship to clinical standards of care, protocol needs, and participant safety.
Provides leadership for direct patient care and protocol adherence collaborating with unit-based nurse management team and study teams.
Acts as a participant advocate. Keeps participants safe in the conduct of clinical research, research interventions and protocol activities. Continually assesses risk and coordinates research activities to minimize participant risk.
Assures consent is completed prior to visit activities.
Design and implement participant/family health education activities for clinical research. Supports participant/family/educational activities.
Serves as an educational and clinical resource or consultant for clinical research participants, family and research staff.
Ensures that nursing practice is safe, effective, efficient and patient centered. Identifies barriers and opportunities to improve protocol adherence and data collection.
Recommends strategies to improve nursing quality and operationalization of required protocol activities.

For a full job description, please send an e-mail to the contact listed below.

About ICTS: The Institute for Clinical and Translational Science (ICTS) at the University of Iowa was approved by the Iowa Board of Regents in 2007 to support the work of investigators involved in clinical and translational science. Our mission is to accelerate translational science through programs to develop the translational workforce, to promote engagement of community members and other stakeholders, to promote research integration across the lifespan, and to catalyze innovative clinical and translational research. These efforts will lead to the development of novel therapies and healthcare delivery strategies, the integration of translational research and clinical practice, and, ultimately to measurable improvements in the health of Iowa and the nation.

Percent of Time: 100%
Pay Grade: 5A
https://hr.uiowa.edu/pay/guide-pay-plans

Benefits Highlights:

Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
For more information about Why Iowa?, click here

Qualifications

Required Qualifications

A Bachelor’s degree in Nursing or an equivalent combination of education and experience.
Current license to practice nursing in Iowa is required by date of hire.
A minimum of 3 years of acute care nursing experience within the last 5 years.
Excellent written and verbal communication skills.
Ability to work occasional weekends, evenings or nights.
General computer skills.

Desirable Qualifications

Epic Experience.
Pediatric nursing or oncology nursing care experience.
Professional certification in a related field of nursing or research.
Knowledge of University of Iowa Hospitals and Clinics policies, procedures and regulations.
Knowledge of Clinical Research, GCP and IRB regulations.
Strong clinical nursing skills including: IV insertion, phlebotomy and assessment.
ACLS and/or PALS certified.

Application Process:

In order to be considered for an interview, applicants must upload the following documents and mark them as a “Relevant File” to the submission:

Resume

Cover Letter

Job openings are posted for a minimum of 7 calendar days and may be removed from positing and filled any time after the original posting period has ended.

Successful candidates will be required to self -disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.Hybrid within Iowa: This position is eligible for a combination of on-campus and remote work. Remote work must be performed at a location within the state of Iowa and comply with the remote work program and related policies.

Remote within Iowa: This position is eligible for primarily remote work but may require limited work onsite at times. Remote work must be performed at a location within the state of Iowa and comply with the remote work program and related policies.

As previously discussed, this position is eligible for hybrid work within Iowa and will require a work arrangement form to be completed upon the start of your employment. Per policy, work arrangements will be reviewed annually, and must comply with the remote work program and related policies and employee travel policy when working at a remote location.

For additional questions, please contact Amy Stewart at amy-stewart@uiowa.edu

This position is not eligible for University sponsorship for employment authorization.

Primary Location

: Iowa City

Job

: Research

Organization

: Healthcare

Schedule

: Regular Full-time

Job Posting

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Company Description

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

Job Description

As a Clinical Research Associate at PSI, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Full-time office-based in Tbilisi, Georgia

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
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

MD
Experience working in a clinical site as a study coordinator or sub-investigator is a plus
Independent on-site monitoring experience in Georgia
Full working proficiency in English and Georgian
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel

Additional Information

PSI is a stable, privately-owned company, organically growing since 1995
We have an excellent reputation in the industry, having won the CRO Leadership awards several years in a row
Team collaboration is high on our agenda. Our aim is for employees to feel valued and heard in friendly and supportive teams
We offer extensive training programs, profound therapeutic area trainings, monitors training program, mentorship programs, interactive soft-skills trainings and more
PSI CRAs have an opportunity to work with different Sponsors on a variety of therapeutic areas
We have a large portfolio of projects, mostly phase II and III
Each monitor will work on a limited number of protocols, thus ensuring they can give the best support to the sites
We have comfortable office facilities with easy commute, corporate benefits, refreshers and team building events

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Synthesis R&D:

Responsible to perform routine organic synthesis. (mg to gram scale) & work independently under the guidance of the leader.
Independently support the scientific team with instrumentation and equipment operation and maintenance.
Able to understand & interpret various instruments like NMR, Mass, HPLC.
Instrument purification like Combiflash, big columns, column packing. Deciding the mobile phase for purification.
Independently handling all types of glassware assembly arrangement, reaction reagent charging, maintaining temperature, nitrogen, etc.
Should be able to understand the written instruction from the scientist including patents and reprints where procedure highlighted by scientists.
To train and support the team members.
Meticulous Documentation & proper data management.
To maintain the record book of the work done like purification or reaction.

ADC (Antibody Drug Conjugate) R&D

Synthesis and purification of complex antibody drug conjugate (ADC) molecules
Synthesis of different type of linkers - using natural and un-natural amino acids, PEGs
Synthesis of high potent drug molecules – payloads
Purification of complex and large molecules by flash column and HPLC
Handling various type chemistry with different payloads
Interpretation and characterization of higher molecular weight compounds

Requirements

Minimum of 1 year to 4 years of experience working in CRO Industry.
Strong organizational, project management and problem-solving skills with impeccable multi-tasking abilities.
Exceptional Interpersonal Skills.
Friendly and professional demeanor.
Ability to write reports and prepare spreadsheets and presentations.
Excellent organizational skills with an ability to think proactively and prioritize work.
Proactive, highly motivated with a \"can-do\" attitude.
Strong and accurate attention to detail.

","hiringOrganization":{"@type":"Organization","name":"o2h Group","sameAs":"https://o2h.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Ahmedabad, Gujarāt, India","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":30,"item":{"@type":"JobPosting","title":"Clinical Research Associate II","datePosted":"2025-09-23","description":"

Company Description

PSI is a leading Contract Research Organization with more than 22 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

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
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 or an equivalent combination of education, training & experience
Independent on-site monitoring experience in France
Experience in all types of monitoring visits in Phase II and/or III
Experience in oncology, hemophilia, infectious diseases, GI
Full working proficiency in English
Proficiency in MS Office applications
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.

We Offer:

Big professional advancement opportunity within Clinical Operations with specific mentorship and training program
Development opportunities across PSI departments
Flexible working hours
Home-office option available, as well as combination of home and office work arrangement
Extensive onboarding trainings and professional development training programs
Highly developed company culture and positive team atmosphere
Additional leave days (12 days of RTT)

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Job Description

Job Profile

Research Associate

Location: Mumbai, India

About This Job.

Research Associate will be responsible for gathering, validating, and formatting the data. This data/charts will support the commercial teams to build insights and recommendations in market research studies. He/she will co-ordinate across internal teams in this regard and support the commercial teams for the clients’ projects and queries by working through databases whenever required.

Responsibilities

Executing tasks to help with link checking for surveys, plus data QC and table formatting of survey results in excel.
Working closely with Commercial consulting teams in a collaborative way for charting data in powerpoint, using analysis plans provided to them.
Adhering to Performance KPIs to ensure quality performances (on-time delivery and data accuracy) and maintain work discipline.
Meeting internal & external deadlines for all deliverables.
Operate in a hybrid physical-virtual and multi-cultural environment, liaising with stakeholders and colleagues.

A Little Bit About You

Intellectual curiosity and persistence while paying attention to details, to find answers to questions and ability to autonomously manage simultaneous tasks/ projects in a fast-paced business environment.

Qualifications

Graduation degree in Commerce, Statistics, Mathematics, Economics, or related field a must.
Good Practical knowledge of Excel and PowerPoint
Excellent numerical skills
Very good interpersonal skills
Good organization skills, meeting deadlines, and team player
Strong business acumen
English language proficiency: writing and verbal
Knowledge of New Product Development Research preferred
Working in North America Shift (2PM-11PM)

Additional Information

Our Benefits

Flexible working environment
Volunteer time off
LinkedIn Learning
Employee-Assistance-Program (EAP)

About Niq

NIQ is the world’s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights—delivered with advanced analytics through state-of-the-art platforms—NIQ delivers the Full View™. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world’s population.

For more information, visit NIQ.com
Want to keep up with our latest updates?
Follow us on: LinkedIn | Instagram | Twitter | Facebook
Our commitment to Diversity, Equity, and Inclusion

At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news-center/diversity-inclusion

","hiringOrganization":{"@type":"Organization","name":"NielsenIQ","sameAs":"https://nielseniq.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Mumbai, MH, India","addressCountry":"India","addressRegion":"Asia/Pacific"}}}},{"@type":"ListItem","position":32,"item":{"@type":"JobPosting","title":"Research Associate, Hibernation","datePosted":"2025-09-23","description":"Until is a moonshot company building a “pause button” for biology. Our near-term focus is organ-scale reversible cryopreservation: preserving donated organs at subzero temperatures without ice formation, then rewarming them uniformly for transplant. By solving this grand challenge, we’re laying the foundation for whole-body reversible cryopreservation, giving patients a bridge to future cures.
To achieve our goal, we are assembling an interdisciplinary team to develop perfusion systems, cryoprotectant formulations, and vitrification and rewarming hardware.
We envision a future where no transplantable organ is lost to logistics, and no terminal diagnosis is final because patients can safely wait for future medicine to arrive.
About the RoleWe are seeking an experienced, motivated and detail-oriented full-time Research Associate to join our hibernation team. In this role, you will contribute directly to advancing our mission by developing and refining whole-body cryoprotectant perfusion protocols. Your initial responsibilities will center on systematic evaluation of perfusion efficiency and post-perfusion organ viability. The person in this role is encouraged to take on significant ownership of specific technical challenges.
You will work closely with scientists, applying fundamental principles from biology, physics, and chemistry to solve complex problems. We value creative engagement and encourage you to explore new ideas, methods, and approaches that can accelerate discovery and optimization.\n

Key Responsibilities

Support and conduct whole-body perfusion experiments, including monitoring physiological parameters, controlling perfusion conditions, and maintaining detailed documentation.
Evaluate multiple tissues and organs post-perfusion, assessing both structural integrity and cryoprotectant distribution across different organ systems.
Ensure accurate sample processing and on-time data reporting.
Review relevant literature and design experimental tests to address key questions that advance and optimize preservation protocols.

Qualifications

Bachelor’s degree in a STEM field (or equivalent STEM-related training and experience).Extensive hands-on experience with in vivo rodent models.
Background or strong interest in physiology, with a creative approach to understanding and manipulating organ function.
Self-driven, resourceful, and motivated by discovery—committed to advancing ambitious scientific projects and pushing the boundaries of knowledge.
At least 2 years of experience with a strong track record of success in executing complex and demanding laboratory procedures.
Demonstrated enthusiasm for problem-solving and for exploring novel protocols and research directions.

Benefits

Direct impact in a moonshot company creating the future as an early team member.
Generous medical, dental and vision insurance coverage.
Flexible time off and paid holidays.
Competitive compensation package, including salary and equity.
Access to a 401(k) retirement savings plan.
FSA and commuter benefits.
Subsidized lunch daily.

As an equal opportunity employer, Until is committed to providing employment opportunities to all individuals. All applicants for positions at Until will be treated without regard to race, color, ethnicity, religion, sex, gender, gender identity and expression, sexual orientation, national origin, disability, age, marital status, veteran status, pregnancy, or any other basis prohibited by applicable law.","hiringOrganization":{"@type":"Organization","name":"Until","sameAs":"https://www.untillabs.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bay Area","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":33,"item":{"@type":"JobPosting","title":"Research Associate II","datePosted":"2025-09-23","description":"

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Essential Duties And Responsibilities:

Independently and successfully execute experiments towards method development, method validation, specifically for extractable and leachable profiling studies, within specified timelines.
Make sound technical recommendations in routine analytical activities. Provide analysis/redesign of key experimental procedures.
Produce scientific experimental data based on written procedures like method of analysis, protocols etc.
Involve in and conduct trouble shooting of analytical methods, laboratory investigations etc
Provide input to select analytical techniques and procedures to solve problems within area of responsibility.
Apply technical theories and principles to projects within area of expertise.
Independently analyze and propose solutions to research challenges. Learn newer analytical techniques to enhance the capability and productivity.
Author documents like Method of analysis/ protocols/ reports
Perform/ provide support as needed in calibration and maintenance of equipment in the laboratory.
Participate and take ownership of equipment installation and qualification activities as per Baxter’s QMS.
Document laboratory work performed per Baxter’s GDP.
Work according to appropriate quality standards and quality principle (e.g., Data Integrity, ALCOA)
Follow Baxter’s Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement.

Qualifications:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Following knowledge, skills, and/or abilities required

N/A: Intern or Co-op

Hands-on experience in chromatographic and/ or spectral techniques like LC-MS/MS, GC-MS, and/or ICP-MS/ ICP-OES.
Operation of analytical tools/ instruments (weighing balances, pH meters etc.) and wet chemistry sample preparation techniques.
Should have analytical problem-solving skills, high learning agility, innovative experimental attitude along with good presentation skills.
Excellent written and verbal communication skills in English.
Demonstrates an inclusive attitude and an ability to collaborate with team members and cross-functional team members for project deliverables.
Ability to objectively assess, organize, and clearly communicate information.
Ability to interpret available information and make recommendations to resolve technical challenges.
Ability to appropriately prioritize work assigned to meet project deliverables in a timely manner.
Provide and accept critical feedback from others in a constructive manner.
Adapt to changes and have an agile mindset.
Embrace diversity and inclusion, value differences.

Education And/Or Experience:

Educational Qualification: Postgraduate/ Ph. D. in Pharmacy/ Chemistry or related field (M. Pharm./ M. Sc./ Ph. D.)
Professional Experience: 4-8 years of relevant experience

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

Recruitment Fraud Notice

Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

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Position Details

2 Year Contract | Full-Time
Academic Level A | $88,842 - $107,666 p.a.
Academic Level B | $113,211 - $133,974 pa.
Location: Bedford Park / Kaurna Country
Level A Position Description
Level B Position Description

The successful candidate will be appointed to either the Level A or Level B position. Please indicate on your application which position(s) you would like to be considered for.

College of Medicine and Public Health

At the College of Medicine and Public Health, we deliver clinical, population and lab-based research, integrated teaching programs and high-quality clinical services. Our footprint reaches out from our world class teaching hospital at the Flinders Medical Centre in South Australia to multiple rural clinical locations all the way to Darwin in the Northern Territory. Our research and teaching equip the next generation of leaders and innovators with the skill, commitment, and vision to protect vulnerable communities and truly advance health outcomes. It is at the heart of everything we do.

About the Research Associate Role (Level A)

We are seeking a Research Associate to contribute to a dynamic research program in Reproductive and Perinatal Pharmacoepidemiology, working under the guidance of the research group lead. The Reproductive and Perinatal Pharmacoepidemiology Research Group is dedicated to improving the health of women and children by advancing the quality, safety, and effectiveness of medication use across the reproductive lifespan — from menstrual health and contraception to pregnancy, lactation, and menopause.

In this role, you will support a range of projects by managing and analysing data from clinical trials, cohort studies, and large linked administrative datasets. You will contribute to study design and implementation, perform statistical analyses, and help prepare high-quality publications, reports, and conference presentations that influence policy and clinical practice.

You may also contribute to the development of grant applications and assist in mentoring students involved in the research program, in line with the University’s policies and academic standards.

About You

To be successful in this role you will demonstrate:

Completion of a PhD or substantial progress toward a PhD in epidemiology, biostatistics, or a related discipline.
Experience working with health data from clinical trials, cohort studies, or large administrative health datasets.
Familiarity with quantitative research methods and their application in health research.
Ability to critically appraise and synthesise literature relevant to reproductive and perinatal health.
Demonstrated capacity to contribute to team-based research and maintain productive professional relationships.
About the Research Fellow Role (Level B)

We are seeking a Research Fellow to join our Reproductive and Perinatal Pharmacoepidemiology Research Group. Working under the direction of the group lead, you will contribute to research aimed at improving the quality, safety, and effectiveness of medication use across the reproductive lifespan.

The role involves managing and analysing data from clinical trials, cohort studies, and large linked datasets. You will support study design, contribute to publications, present findings at conferences, and assist in preparing research funding applications. This is a great opportunity to be part of a collaborative team making a real impact on women's and children’s health.

About You

To be successful in this role you will demonstrate:

Postgraduate or PhD qualifications in epidemiology, statistics, biostatistics, public health, with a strong component in epidemiology and biostatistics, or a related degree
Research experience in terms of publications in high quality journals, attraction of external competitive grants and presentations at a national and/or international level, preferably related to reproductive/perinatal health.
Ability to work with health data collected through primary data collection (e.g. clinical trials and cohort studies) or the use of large administrative health datasets.
Interpersonal skills and experience in collaborating and engaging with diverse stakeholders and industry partners.
Excellent analytical skills with the ability to collect, organise, and analyse health related data with attention to detail and accuracy.
Experience to undertake collaborative research and establish and maintain effective relationships with staff and industry.

Life At Flinders

We're transforming and investing in people and facilities to create contemporary, stimulating, and satisfying learning and work environments that reflect our core values of excellence, innovation, courage, and integrity. Flinders is refocusing its strategic priorities with the aim of elevating its performance to be a top ten Australian university, and amongst the top 1% in the world.

Reaching beyond the limits of buildings, borders, and backgrounds, ours is an inclusive culture that believes absolutely in equality and opportunity for all. We don't just accommodate differences; we embrace and celebrate them. So, why work at Flinders?

17% Superannuation + salary packaging options
Flexible Working Arrangements
Wide range of professional development activities and services
We embrace diversity and promote equity and inclusion for all students and staff
Vibrant campus life and amenities including on campus health care services, gym and childcare centre (Bedford Park, South Australia).

Our Commitment to Reconciliation and Indigenous Employment

Flinders University is proud to be an organisation that is committed to our Reconciliation Action Plan and Indigenous Workforce Strategy. Our vision is to be a preferred employer for Aboriginal and Torres Strait Islander peoples. We are committed to progressing Indigenous advancement in education, research, employment, and wellbeing, and strongly encourage applications from Aboriginal and Torres Strait Islander peoples for all Flinders vacancies.

Prescribed Conditions for Employment

A current Nationally Coordinated Criminal History Check which is satisfactory to the University will be required by Flinders University before the successful applicant can commence in this position. A criminal record will not automatically disqualify a candidate from consideration. Each case will be assessed on its individual merits and relevance to the inherent requirements of the role.
Please note that you may be required to provide evidence that you are up to date with COVID-19 vaccinations, in line with the Flinders University COVID-19 Vaccination Policy
It is a requirement of this position that the incumbent maintain a current Working with Children Check which is satisfactory to the University in accordance with the Child Safety (Prohibited Persons) Act 2016 (SA).

How to Apply and Information

You are required to submit your CV and a Suitability Statement of no more than 3 pages, addressing the Key Position Capabilities of the Level A Position Description or Level B Position Description
For more information regarding this position, please contact Luke Grzeskowiak
Please see here for our Reconciliation Action Plan
Please see here for our Indigenous Workforce Strategy
Applications to be submitted before 10.00pm:

Certification

07 Oct 2025

At Flinders we embrace and celebrate diversity and encourage applications from Aboriginal and Torres Strait Islander peoples, and people of all ages, ethnicities, abilities, sexual orientations, and gender identities.

Flinders. Fearless.

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Band

Level 3

Job Description Summary

Location: This role is field based (home office) and requires national travel.

Relocation support: Novartis is unable to offer relocation support: please only apply if accessible.

Step into a role where your work truly matters. As a Clinical Research Associate (CRA) at Novartis, you’ll help advance innovative treatments by ensuring excellence in clinical trial execution. Working within Study & Site Operations in Global Drug Development (GDD), you’ll manage site relationships and oversee on-site and remote monitoring from initiation through completion of Phase I–IV trials. You’ll ensure compliance with ICH/GCP, local regulations, and SOPs, while proactively managing site performance, recruitment, and quality. As the main point of contact for sites, you’ll identify needs early and resolve issues efficiently. Join a passionate team, support breakthrough science, and help deliver life-changing therapies to patients faster.

This position is part of the Study & Site Operations (SSO) EMEA GBR Field Monitor Management team and reports directly to CRA Manager.

#LI-Hybrid

Job Description

Key Responsibilities:

Manage study sites to ensure compliance with protocols, regulations, and Novartis procedures
Conduct site initiation visits and deliver tailored training to site personnel
Perform ongoing site monitoring to ensure data quality and patient safety
Implement site management strategies to address compliance and operational issues
Maintain accurate and timely documentation of all monitoring activities
Ensure continuous updates to global and local electronic systems
Identify, resolve, and escalate site-related issues as appropriate
Maintain up-to-date Trial Master Files and collect essential site documents
Support audit and inspection readiness, ensuring timely corrective actions
Collaborate with internal teams to support recruitment and contingency planning

Essential Requirements:

Degree in a scientific or health-related discipline; advanced degree preferred
Fluent in written and spoken English
Up to two years of experience in clinical research, with focus on monitoring and trial execution
Strong knowledge of international standards including GCP and ICH
Proven ability to manage sites independently and resolve issues proactively
Willingness and ability to travel domestically and internationally as needed
Full UK driving license

Desirable Requirements:

Experience working in a global pharmaceutical or CRO environment

Commitment To Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Skills Desired

Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences","hiringOrganization":{"@type":"Organization","name":"Novartis","sameAs":"https://www.novartis.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Field Force (England / Wales), United Kingdom","addressCountry":"United Kingdom","addressRegion":"Europe"}}}},{"@type":"ListItem","position":36,"item":{"@type":"JobPosting","title":"Clinical Research Associate - Central/East Coast","datePosted":"2025-09-23","description":"Clinical Research Associate - Central/Eastern

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 to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

What you will be doing

Minimum of 12 months of experience as a Clinical Research Associate.
Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Your Profile

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers 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.

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

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What you will be doing

Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Your Profile

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers 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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The Fixed Income Research Associate will work primarily in the municipal bond universe, providing fundamental analysis of various credits. The Investment analysis performed will include interpreting market data, trends and economic forecasts. Cash flow modeling and financial reporting analysis are essential. The Fixed Income Research Associate will assist senior analysts with crafting and implementing investment theses.

Responsibilities

Analyze individual municipal credits, interpret market and industry trends, and examine specified market sector activity to provide information and analysis required in the investment decision-making process.
Complete fundamental analysis on specific municipal credits and create/update investment models with specific issuer information, income statements/ balance-sheet numbers and market trend data. Based on analysis make recommendations and articulate those buy, sell, hold recommendations with senior investment staff.
Research and recommend new sources of information to more senior investment staff.
Contribute to credit analysis and/or analysis of classes of securities, market trends, yield and duration relationships, and pricing trends between different fixed-income sectors.
Assist in various functions that support the whole credit research team such as compiling research data on holdings.
May support more than one investment strategy team; foster relationships with various portfolio management teams to effectively do so.
All functions must be performed in the context of the unique client-defined investment strategy and the work contributes to the strategy’s successful performance and the Company’s ability to raise assets. The investment analysis performed include fundamental analysis of individual municipal credits and interpreting market data, trends and economic forecasts.

Qualifications

Bachelor’s degree required; May hold advanced degree and/or CFA designation or progress towards either.
Typically has 3-5 years of experience in dedicated investment analysis experience in the municipal market.
Superior organizational and analytic skills to complete detailed fundamental analysis. Ability to construct investment models to identify and track value added securities.
Strong written and verbal communication skills to deliver reviews and recommendations. Ability to articulate highly technical information with conviction.
Sense of judgment and self-discipline in order to evaluate multiple opportunities and make appropriate investment decisions.
Strong understanding of business and economics in order to research target companies and determine potentially profitable investments.
Ability to work well with multiple levels of internal and external contacts; strong communications skills to effectively convey recommendations & rationale.
Good understanding of business and economics in order to research target credits and recommend potentially profitable investments.
Coding abilities a plus.
Experience analyzing High Yield Municipal credits a plus

When You Join Our Team:

We’ll empower you to learn and grow the career you want.
We’ll recognize and support you in a flexible environment where well-being and inclusion are more than just words.
As part of our global team, we’ll support you in shaping the future you want to see

About Manulife and John Hancock

Manulife Financial Corporation is a leading international financial services provider, helping people make their decisions easier and lives better. To learn more about us, visit https://www.manulife.com/en/about/our-story.html.

Manulife is an Equal Opportunity Employer

At Manulife/John Hancock, we embrace our diversity. We strive to attract, develop and retain a workforce that is as diverse as the customers we serve and to foster an inclusive work environment that embraces the strength of cultures and individuals. We are committed to fair recruitment, retention, advancement and compensation, and we administer all of our practices and programs without discrimination on the basis of race, ancestry, place of origin, colour, ethnic origin, citizenship, religion or religious beliefs, creed, sex (including pregnancy and pregnancy-related conditions), sexual orientation, genetic characteristics, veteran status, gender identity, gender expression, age, marital status, family status, disability, or any other ground protected by applicable law.

It is our priority to remove barriers to provide equal access to employment. A Human Resources representative will work with applicants who request a reasonable accommodation during the application process. All information shared during the accommodation request process will be stored and used in a manner that is consistent with applicable laws and Manulife/John Hancock policies. To request a reasonable accommodation in the application process, contact recruitment@manulife.com.

Referenced Salary Location

Boston, Massachusetts

Working Arrangement

Hybrid

Salary range is expected to be between

$91,000.00 USD - $165,000.00 USD

If you are applying for this role outside of the primary location, please contact recruitment@manulife.com for the salary range for your location. The actual salary will vary depending on local market conditions, geography and relevant job-related factors such as knowledge, skills, qualifications, experience, and education/training. Employees also have the opportunity to participate in incentive programs and earn incentive compensation tied to business and individual performance.

Manulife/John Hancock offers eligible employees a wide array of customizable benefits, including health, dental, mental health, vision, short- and long-term disability, life and AD&D insurance coverage, adoption/surrogacy and wellness benefits, and employee/family assistance plans. We also offer eligible employees various retirement savings plans (including pension/401(k) savings plans and a global share ownership plan with employer matching contributions) and financial education and counseling resources. Our generous paid time off program in the U.S. includes up to 11 paid holidays, 3 personal days, 150 hours of vacation, and 40 hours of sick time (or more where required by law) each year, and we offer the full range of statutory leaves of absence.

Know Your Rights I Family & Medical Leave I Employee Polygraph Protection I Right to Work I E-Verify I Pay Transparency

Company: John Hancock Life Insurance Company (U.S.A.)","hiringOrganization":{"@type":"Organization","name":"Manulife","sameAs":"https://www.manulife.com/"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"USA, Massachusetts, Boston, 197 Clarendon Street, United States","addressCountry":"United States","addressRegion":"North America"}}}},{"@type":"ListItem","position":39,"item":{"@type":"JobPosting","title":"Postdoctoral Research Associate - Pathology","datePosted":"2025-09-23","description":"The Klco lab is looking for a post-doctoral fellow interested in using mouse and human models to understand pediatric AML and MDS. We are part of the Department of Pathology and the Center of Excellence for Leukemia Studies with access to cutting-edge technology and resources.

The successful candidate will ideally have a PhD (or will obtain a PhD) with a focus on molecular biology, cancer or genomics. Specific experience in mouse models and hematopoietic development are a plus.

St. Jude Children’s Research Hospital is a world-class research institution dedicated to pediatric cancer and other catastrophic diseases of childhood. The first and only National Cancer Institute (NCI)-designated Comprehensive Cancer Center devoted solely to children. Our 300 faculty work across the spectrum of basic, translational, clinical, and population science in a highly collaborative multidisciplinary environment that includes a Nobel laureate and members of the National Academy of Science and the National Academy of Medicine. St. Jude is ranked on Fortune Magazine’s “Best Workplaces in Health Care & Biopharma” and Glassdoor’s “Best Places to Work,” and is located in the heart of Memphis, Tennessee, a vibrant and friendly city at the historic American crossroads of music, trade, food and culture.

We are in pursuit of the brightest minds in biomedical sciences, individuals poised to contribute to our research progress. Other than access to top-quality scientists and mentors, as a postdoctoral trainee at St. Jude, you will have:

A Blend of Academic Freedom and Industrial Efficiency: Access to shared resources and facilities led by expert scientists, coupled with cutting-edge technology, accelerates research productivity.
Customized Professional and Career Growth: Experience specifically designed programs to enhance professional growth and career readiness empowering postdocs for success beyond their training. This includes access to grant writing workshops, individual development plans, teaching and mentoring opportunities, non-research career advancement programs, professional development allowance, and so much more.
Competitive Compensation: Embark on your journey with a competitive salary starting at $72,500 a year, comprehensive benefits and generous relocation assistance, reflecting our commitment to recognize and invest in talent.

A Sense of Community: St. Jude fosters a vibrant postdoc community that supports a well-balanced life. A dynamic environment promotes connections and camaraderie among postdocs from all backgrounds.

St. Jude is an Equal Opportunity Employer

No Search Firms

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A postdoctoral fellowship in medicinal chemistry is available in the laboratory of Dr. Richard Lee to perform structure-based drug design and synthesis of drug candidates as part of an interdisciplinary research team. The ideal candidate will have a strong background in medicinal chemistry and chemical biology. The candidate will be responsible for the design and synthesis of lead optimization series using emerging structure-activity relationships that consider both target and drug metabolism factors. Experience in antibiotic chemistry, CNS drug discovery, computer-aided drug design, ADME and PK profiling, LC-MS, and NMR analysis would be advantageous. The successful candidate must be an effective communicator and team player, keep an accurate notebook, and maintain a safe working environment.

Postdoctoral trainees in the Department of Chemical Biology and Therapeutics have access to outstanding facilities for inhibitor discovery, including access to large chemical screening libraries; analytical chemistry and ADME support; high-throughput and biophysical screening capabilities; and high-resolution structural biology, including crystallography, NMR spectroscopy, and cryo-electron microscopy. Each fellow has access to a dedicated fume hood and rotavap, electronic notebook, Biotage flash chromatography system, NMR, and UPLC-MS.

Eligibility: A recent PhD. in medicinal chemistry, chemical biology, or organic chemistry is required. The successful applicant will be a good communicator in oral and written English with a track record of publication in top chemistry journals and a proven record of chemical synthesis.

St. Jude is an Equal Opportunity Employer

No Search Firms

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What you will be doing

Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Your Profile

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers 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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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.
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

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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We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate 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.
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

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

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.
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

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":"Netherlands, Utrecht, Zen","addressCountry":"The Netherlands","addressRegion":"Europe"}}}},{"@type":"ListItem","position":45,"item":{"@type":"JobPosting","title":"Clinical Research Associate - Central/East Coast","datePosted":"2025-09-23","description":"Clinical Research Associate - Central/East Coast

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.
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

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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About This Role:

Wells Fargo is seeking a Securities Research Associate

In This Role, You Will:

Provide support in the editing and publishing functions within the Global Research and Economics Group in Wells Fargo Securities
Generate research packet products, post research documents to market data vendors, update and maintain mailing lists, and provide client access to web sites
Assign reports to Editors and Supervisory Analysts to ensure the most efficient use of resources
Maintain databases
Receive direction from leaders
Exercise independent judgment while developing the knowledge to understand function, policies, procedures, and compliance requirements
Collaborate and consult with peers, colleagues and managers to resolve issues and achieve goals

Required Qualifications:

2+ years of Securities Research experience, or equivalent demonstrated through one or a combination of the following: work experience, training, military experience, education

Desired Qualifications:

MBA, CA, CFA or master’s in finance from a premier education institute
2+ years’ experience in Corporate Banking, Investment Banking
Experience in working in any of the following sectors preferably, FIG&/or Banks
Strong inclination towards building a career in Corporate Banking, Corporate Finance, Investment Banking or Capital Markets
Good understanding of Credit metrics, Covenants, Capital structure, financial statement and ratio analysis
Impeccable communication and interpersonal relationship skills with the ability to interact with senior professionals and key stakeholders
Strong logical, analytical skills and a systematic problem-solving approach
Ability to proficiently use Microsoft Office Applications – Power Point and Excel
Strong time management skills and ability to work under pressure and meet strict deadlines
Attention to detail and ability to ensure high quality of deliverables
Ability to interact with integrity and a high level of professionalism with all levels of team members and management
Results driven, accountable and ability to work with multiple priorities in a fast-paced and results-driven environment

Job Expectations:

Work as an individual contributor on various work streams that form key components of Wells Fargo’s Corporate Banking debt financing, F/X and/or Rates products, across sectors
Assist in preparing Credit memos, credit reports or annual reviews for corporate clients including support in drafting company/borrower overviews, business description, industry overviews, corporate actions and in performing historical financial analysis and industry or peer analysis
Work on publishing Quarterly or annual earnings summaries for target portfolio companies and in tracking credit rating reports or equity reports
Prepare market or sector updates, sector newsletters to keep a track of key market developments
Work on borrower rating, capital structure and covenant analysis
Monitor and track covenant compliance
Support in drafting non-borrower reports, Annual credit reviews or CAC Memos
Develop excellent working knowledge of market database tools e.g. Fact set, Thomson one, Capital IQ, Moody’s, S&P etc.
Interact with multiple stakeholders to achieve the desired goal

Posting End Date:

29 Sep 2025

*Job posting may come down early due to volume of applicants.

We Value Equal Opportunity

Applicants With Disabilities

To request a medical accommodation during the application or interview process, visit Disability Inclusion at Wells Fargo.

Drug and Alcohol Policy

Wells Fargo maintains a drug free workplace. Please see our Drug and Alcohol Policy to learn more.

Wells Fargo Recruitment and Hiring Requirements:

Third-Party recordings are prohibited unless authorized by Wells Fargo.
Wells Fargo requires you to directly represent your own experiences during the recruiting and hiring process.

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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.
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

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

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.
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

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.
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Job Title:

Clinical Research Associate Coordinator

Department:

FAES | Food Science and Technology-JM

The Clinical Research Coordinator supports and implements daily clinical research activities across one or more projects in nutritional, dietetic, biological, and health sciences. This role involves participant recruitment, data collection and analysis, administration of cognitive and behavioral assessments, and coordination with interdisciplinary teams to ensure protocol compliance and research integrity.

Key Responsibilities:

Conduct clinical research activities in accordance with approved protocols
Assist in data collection, coding, extraction, and analysis
Evaluate and calculate standardized scoring for diagnostic, psychological, and behavioral assessments
Support the development and tailoring of cognitive tests per study protocols
Maintain access and credentials for the NIH Cognitive Toolbox
Identify and recruit study participants, including travel to medical centers and clinics
Educate healthcare providers on study protocols and goals
Interview, assess, enroll participants, and administer study questionnaires and measurements
Train and supervise students and research personnel
Contribute to achieving study goals and maintaining compliance with clinical protocol requirements

Minimum Required Qualifications:

Bachelor’s degree in Biological Sciences, Health Sciences, Social Sciences, or a related medical field, or equivalent combination of education and experience
0–2 years of relevant experience preferred
Ability to apply academic and/or practical knowledge to biological/health/nutrition science research
Familiarity with clinical measurements and cognitive/behavioral testing protocols
Strong organizational skills and attention to detail
Excellent written, verbal, and interpersonal communication skills
Ability to problem-solve, take initiative, and make recommendations

Preferred Qualifications:

Advanced Practice Registered Nurse (APRN) and Psychiatric-Mental Health Nurse Practitioner (PMHNP) credentials
Experience conducting clinical research in food science, nutrition, health, or dietetics
Experience administering cognitive and behavioral questionnaires

Additional Information:

This job profile is a Clinical Research Specialist 1 (S1 level) position on the career roadmap.
The offer for this position will fall within this range based on internal equity, unit’s available budget, and the candidate’s qualifications

Location:

Parker Food Science and Technology (0064)

Position Type:

Intermittent

Scheduled Hours:

0.2

Shift:

Varying Shifts

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.

The university is an equal opportunity employer, including veterans and disability.

As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.

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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.

Parexel FSP is hiring Senior Clinical Research Associates to join us on

A Permanent,Home-Based Basis.

Dedicated to a single sponsor in BioPharma, who is revolutionizing healthcare by harnessing the power of science to benefit people, society, and the planet. Turkey is a vital part of their global network, hosting colleagues from every segment of the life sciences value chain. Their science-driven approach aims to transform healthcare and improve patient outcomes, while also fulfilling a purpose-led role in society.

Job Purpose:

As a Senior Clinical Research Associate (CRA)/Clinical Monitor, you will have local responsibility for the delivery of the studies at allocated sites and will be an active participant in the local study team(s). You will work in close collaboration with other Monitors and the Local Study Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. You will be the main contact with the study site and will have responsibility for the proper conduct of the study.

The SCRA is responsible for the preparation, initiation, monitoring, and closure of an agreed number of centers in clinical studies according to Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations, and that the centers deliver according to the commitment in the individual trials.

A SCRA with longer tenure and experience may take on additional responsibilities, including tasks associated with the Local Study Manager.

Requirements:

Minimum 3 years of experience as a Clinical Research Associate conducting all visits.
Experience gained ideally in Pharma, CRO, or Biotech.
Good understanding of Clinical Study Management including monitoring, study drug handling, and data management.
Bachelor’s degree in a related discipline, preferably in life science, or equivalent qualification.
Minimum 3 years oncology experience.

Apply Today!

#Li-Ta1

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The Opportunity:

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Higher Education

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