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.
Key Responsibilities:
* 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.
Required Experience:
* 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.
Additional Details:
* 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.
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