We're Hiring: Clinical Research Associate - Managed Access Programmes
Location: Weybridge or Burton upon Trent – this is a hybrid role with 2-3 days onsite.
Make an Impact in Patient Access
Are you a clinical operations professional with a passion for making a difference in patients' lives beyond clinical trials? Join Clinigen, a global leader in access to medicines, and take the lead in developing Managed Access Programmes (MAPs) that ensure patients receive critical therapies post-trial or outside of commercial availability.
As a CRA, you'll play a central role in:
✅ Supporting initiation, setup, monitoring, and close-out activities of Open Label Extension Clinical Trials
✅ Ensuring protocol adherence and data integrity across programmes
✅ Acting as key contact for HCPs, investigators, and sites
✅ Defining and documenting clinical processes to support operational excellence
✅ Ensuring full compliance with regulatory standards
✅ Effectively maintaining study documentation and adhering to GCP frameworks
What We’re Looking For:
We’re seeking someone with:
- Life sciences degree (or equivalent experience)
- Hands on experience in CRA role / clinical operations
- Strong understanding of: GCP E6 (R3) and regulatory frameworks, Clinical data collection and monitoring processes
- Effective stakeholder management you’ll be dealing with external sites & HCPs
- Strong attention to detail, organisation skills and documentation discipline
- Knowledge of Trial Master Files and Essential Records
Why Join Clinigen?
At Clinigen, you’ll join a mission-driven team that ensures patients around the world get access to the medicines they need. You’ll work on innovative projects that sit at the intersection of clinical, regulatory, and compassionate use, shaping the future of access to treatment.
Ready to Apply?
Apply directly through LinkedIn or via the Korn Ferry Website.
