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.

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.