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Rho Inc logo

Project Associate

Posted about 2 months ago

RemoteCzechiaEN

Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges.

At Rho, you’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. With a collaborative team of smart, talented, and positive people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve.

As a Project Associate, you will have the opportunity to gain the necessary experience and opportunities to grow your career in Clinical Research! You will assist project managers in day-to-day operations of commercial studies.  Please note that this is an entry-level position and it is not a laboratory research position.

Our Study Teams will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!

The position will offer the opportunity to participate in all aspects of clinical research support, including document preparation, maintenance, and filing; meeting coordination and support; and data management activities including data entry and review.  More specifically, the position may also include the following responsibilities:

  • Writing external correspondence, such as emails, memos, minutes and reports
  • Formatting documents and creating document templates
  • Support Study Team to track the study status, materials, system accesses and study team trainings
  • Creating and formatting Case Report Forms, manual of operations documents, and other study-related documentation
  • Maintaining project website
  • Communicating with internal and external project staff

Requirements

  • Bachelor’s degree in a scientific field or a related area of study with research emphasis; past experience working with data or on research studies is a plus!
  • Strong Communicator: Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho’s.
  • Committed to Quality: Every job at Rho requires an attention to detail, a deep understanding of our high-quality scientific standards, and an ability to care about every outcome.
  • High-Character: Contribute to our collaborative culture with honesty and integrity. At Rho, we value a strong team spirit highlighted by loyalty, accountability, and mutual trust. We work smart together, we work hard together, and we laugh together. We take responsibility for our actions, forgive honest mistakes and respect one another.
  • Critical Thinker: Rho values thinking. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience. We evaluate situations and opportunities objectively and incisively; we then craft novel, practical solutions.
  • Agile and Adaptable: Rho values the ability to change quickly. We eagerly anticipate, respond to, and take advantage of changes in our environment. We embrace risk but manage it by planning, accepting, and learning from both failures and successes. The opportunity to adapt and evolve energizes us.

 Please submit your resume / CV in English. We are excited to hear from you!

Job details
Workplace
Remote
Location
Czechia
Experience
EN

Smarter trials start with strategy. Rho is the global CRO built on science, cohesion, and sponsor-first thinking—from first-in-human to approval.

Employees
787
Industry
Biotechnology Research
Headquarters
Durham, North Carolina
Founded
1984
Company location
2635 E NC Highway 54, Durham, North Carolina 27713, US
Specialties
Clinical Trial Management, IND & NDA Submissions, Protocol Development, Regulatory Strategy, Program Management, Site Selection & Start-up, Adaptive Trial Design, Clinical Monitoring, Biostatistics, Clinical Data Management, CDISC, IVRS, IWR, Randomization, Decentralized & Virtual Clinical Trials, Risk-Based Quality Management, Rare Disease Clinical Trials, Analgesia Clinical Trials, Infectious Disease Clinical Trials, CNS Clinical Trials, Neurology Clinical Trials, and Psychiatry Clinical Trials

Key team members

Michael Gregor

Michael Gregor

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