About the role
CRA II / Senior Clinical Research Associate – French Speaking
Location: UK-based / Remote
Travel: UK-wide, plus France & French-speaking Belgium.
Site visits: 7-8 visits per month
Contract: Permanent, Full-time
Focus: Phase II/III Clinical Trials | Oncology / Rare Disease
Salary: £55,000-£65,000 (Flexible on experience)
CPL Life Science are currently supporting a specialist CRO in the search for an experienced CRA II / Senior CRA to join their Clinical Monitoring team.
This is an excellent opportunity for a CRA with strong Phase II/III monitoring experience who is fluent in English and French and enjoys working across complex clinical trials and international sites.
Key Experience
- Extensive on-site clinical monitoring experience across Phase II and Phase III clinical trials
- Proven experience conducting Pre-Study, Site Initiation, Interim Monitoring and Close-Out Visits
- Strong understanding of site qualification, selection and ongoing site oversight
- Experience assessing investigator sites, including staff, facilities, equipment, resources and study capability
- Confident in providing site staff training and supporting sites throughout the study lifecycle
- Experience identifying, documenting and resolving site issues, protocol deviations and compliance concerns
- Ideally, previous experience working on complex clinical trials, particularly oncology and/or rare disease
- Strong understanding of GCP, clinical trial processes and regulatory requirements
- Excellent communication, collaboration and problem-solving skills,
Strong experience in Oncology trials is essential, as well as fluent French.
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