Are you a passionate and skilled Clinical Trial Associate looking for a flexible, dynamic role? Join a leading Biotech as a Freelance Clinical Trial Associate and contribute to groundbreaking clinical research while enjoying a hybrid work arrangement!
Role Overview: As a Freelance Clinical Trial Associate (CTA), you'll play a key role in supporting the management and execution of clinical trials. You’ll work with a talented team, ensuring the smooth progress of studies, from start-up through to close-out, all while adhering to regulatory standards.
Location:
* London Office (2 days per week)
* Work remotely the rest of the time!
Key Responsibilities:
* Assist in the preparation and submission of study documents.
* Support the management of clinical trial sites and vendors.
* Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
* Maintain study-related documentation and databases.
* Coordinate and communicate with stakeholders, including monitors, investigators, and clinical teams.
Requirements:
* Previous experience as a Clinical Trial Associate (CTA) or similar clinical role.
* Knowledge of clinical trial processes and GCP.
* Strong organizational and communication skills.
* Ability to work independently and as part of a team.
* Availability to be in the office in London for 2 days per week.
Interested? Apply now and be part of an innovative team shaping the future of clinical research!