In-house CRA

In-house CRA – France

Location: Fully remote, anywhere in France

Employment type: Permanent

Model: Dedicated FSP

Travel: Up to 25%

We are seeking an In-house Clinical Research Associate to join Advanced Clinical, working on a dedicated FSP basis with a global biopharmaceutical company.

You will support CRAs and investigational sites across study start-up, trial conduct and close-out, combining remote site oversight with occasional site visits.

Key responsibilities

• Maintain regular site contact to track recruitment, study supplies, data entry and outstanding actions.
• Review EDC remotely and follow up on data queries, including during database lock.
• Support CRAs with site visit preparation and follow-up, including action items and protocol deviations.
• Maintain study systems and perform quality checks of country- and site-level eTMF documentation.
• Support study start-up activities, including site documentation, contract negotiations and ethics submissions.
• Act as back-up for the primary CRA and support site audits and inspections.
• Conduct pre-study and close-out visits independently where approved, and co-monitor as required.

Required experience

• A degree in Life Sciences or a related discipline, or a Registered Nursing qualification.
• At least 2–3 years’ clinical research experience as a sponsor-side Clinical Trial Specialist, Clinical Trial Assistant or Site Coordinator.
• Strong knowledge of ICH-GCP, clinical trial processes and applicable regulatory requirements.
• Experience using EDC, IVRS/IRT and CTMS systems.
• Fluent written and spoken French and English.
• A valid driving licence and willingness to travel up to 25%.