Freelance CRA – UK | French & English Speaking
I’m currently supporting a CRO looking to bring an experienced Freelance CRA onto a part-time, sponsor-dedicated project.
The CRA will be based in the UK and work closely with both the CRO and sponsor teams, supporting sites as part of a global clinical trial. We’re particularly interested in CRAs who have experience working across international studies and ideally have previously supported sites in France.
Key responsibilities:
- Managing monitoring activities across assigned clinical trial sites
- Conducting site initiation, routine monitoring and close-out visits
- Managing site relationships and acting as a key point of contact for investigators and site teams
- Monitoring recruitment, data quality, site performance and key study metrics
- Identifying and escalating site-level risks and supporting resolution of study issues
- Ensuring compliance with the protocol, ICH-GCP and applicable local regulations
- Reviewing source documentation, study documentation and site files
- Supporting study start-up and site activation activities where required
- Completing monitoring reports and study documentation within agreed timelines
Experience required:
- Strong independent CRA and site monitoring experience
- Fluent in French and English
- UK based with the ability to travel for site visits when required
- Experience working on global/multinational clinical trials
- Previous experience monitoring or supporting clinical trial sites in France would be ideal
- Comfortable working across international and cross-functional study teams
- Strong knowledge of ICH-GCP and clinical trial regulations
- Oncology, Rare Disease and/or Neurology experience preferred
Contract details:
- Freelance / contract
- Part-time
- UK based
- Global clinical trial
- Site travel required
If you’re an experienced freelance CRA with French and English language skills and this sounds relevant to your background, please get in touch with your latest CV.
