Join a global leader in access to medicines as a Clinical Research Associate, supporting Managed Access Programmes (MAPs) that give patients access to critical therapies post-trial or outside commercial availability.
You'll be responsible for:
✅ Setup, monitoring & close-out of Open Label Extension trials
✅ Protocol adherence & data integrity
✅ Key contact for HCPs, investigators & sites
✅ Compliance with GCP & regulatory standards
What we need:
🔹 Based in the UK or Paris
🔹 Fluent in both French and English
🔹 Life sciences degree (or equivalent experience)
🔹 CRA / clinical operations experience
🔹 Strong knowledge of GCP E6 (R3), TMFs & Essential Records
🔹 Great stakeholder management & attention to detail
🔹 Willingness to travel to sites a few times a month
Please apply ASAP and you'll be contacted to discuss further!!