Clinical Research Associate

Freelance Site-Based Senior CRA – 12-Month Contract | London

We are looking for an experienced Site-Based Senior Clinical Research Associate (CRA) to join a growing clinical research team on a 12-month freelance contract in London. This is a hands‑on, on‑site role, supporting the operational delivery of clinical trials while ensuring compliance with regulatory standards.

• Manage day‑to‑day clinical trial activities at assigned sites.
• Ensure compliance with study protocols, ICH‑GCP, and UK regulatory requirements.
• Coordinate with Principal Investigators, CROs, sponsors, and internal teams.
• Review source documents and ensure accurate data entry.
• Maintain site documentation and regulatory files.
• Support monitoring visits, audits, and inspections.
• Mentor and train site staff as needed.

• Bachelor’s degree in Life Sciences, Pharmacy, or related field.
• 2–4 years of clinical research experience, including at least 2 years as a CRA.
• Strong knowledge of ICH‑GCP and UK regulatory guidelines.
• Excellent organizational, communication, and interpersonal skills.
• Ability to manage multiple studies simultaneously.

• 12-month freelance contract.
• Full‑time, on‑site role in London.

This is a great opportunity for a motivated CRA to make a tangible impact in a dynamic clinical research environment.