Study Start Up Specialist

2 months ago


Reading, Reading, United Kingdom PRA Full time
About the Role

At PRA, we're committed to advancing human health through innovative clinical research solutions. As a Study Start Up Associate II, you'll play a critical role in ensuring the successful initiation of clinical trials at our research sites.

Key Responsibilities
  • Negotiate and manage clinical trial agreements, budgets, and ancillary agreements with study sites and sponsors.
  • Oversee the preparation and review of contractual documents, including indemnification processes.
  • Establish and maintain effective communication with study sites, sponsors, and internal personnel regarding contract-related matters.
  • Ensure timely negotiation and execution of contracts within agreed parameters.
  • Prepare, review, and negotiate amendments to contracts as required.
  • Conduct quality control reviews of completed contracts prior to execution.
Requirements
  • Bachelor's degree in a related field, such as paralegal studies or law.
  • Desirable experience in study start up or contracts at a Contract Research Organization (CRO).
  • Experience in clinical research with a focus on contract review and negotiation.
What We Offer

PRA is committed to providing a competitive compensation package, including annual bonuses tied to performance goals. We also offer a range of health-related benefits, retirement plans, and other perks to support your well-being and career growth.

We're an equal opportunity employer and welcome applications from diverse candidates. If you require reasonable accommodations during the application process or to perform the essential functions of this role, please let us know.



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