Clinical Project Associate

  • 25 GBP - 25 GBP
  • Uxbridge, United Kingdom
  • Contract
Freelance Clinical Trial Associate Opportunity with Leading Global Pharma - UK Based

Company Overview: Join a dynamic and innovative global pharmaceutical company committed to advancing healthcare through groundbreaking research and development. We are seeking a highly motivated and experienced Freelance Clinical Trial Associate to contribute to our cutting-edge clinical trials.
Position: Freelance Clinical Trial Associate
Location: West London – hybrid (3 days per week)
  • Collaborate with cross-functional teams to support the planning, execution, and closure of clinical trials.
  • Assist in the preparation and maintenance of essential trial documentation, ensuring compliance with regulatory standards and company procedures.
  • Coordinate with investigative sites, vendors, and study personnel to facilitate smooth trial operations.
  • Conduct site qualification, initiation, monitoring, and close-out visits as needed.
  • Ensure timely collection and review of study data, resolving data discrepancies and issues as they arise.
  • Support the preparation of regulatory submissions and responses to health authorities.
  • Strong with Word, PowerPoint, and Excel. Knowledge of FDA and or EMEA Regulations, ICH Guidelines, GCPs, and/or familiarity with standard clinical operating procedures is a plus.
  • Bachelor's degree in a relevant scientific discipline.
  • Proven experience as a Clinical Trial Associate in the pharmaceutical industry.
  • Strong understanding of GCP, ICH guidelines, and regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Proficient in the use of clinical trial management systems and other relevant software.
  • 12 months
How to Apply: Interested candidates should submit their CV and a brief cover letter highlighting their relevant experience to
Laurie Watts Lead Client Partner

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