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.
How to Apply: Interested candidates should submit their CV and a brief cover letter highlighting their relevant experience to email@example.com