Freelance Clinical Trial Associate

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!

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