<div><h3>Were Hiring: Clinical Research Associate - Managed Access Programmes</h3><p>Location: Weybridge or Burton upon Trent – this is a hybrid role with 2-3 days onsite.</p><h3>Make an Impact in Patient Access</h3><p>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.</p><h3>As a CRA, youll play a central role in:</h3><ul><li>Supporting initiation, setup, monitoring, and close-out activities of Open Label Extension Clinical Trials</li><li>Ensuring protocol adherence and data integrity across programmes</li><li>Acting as key contact for HCPs, investigators, and sites</li><li>Defining and documenting clinical processes to support operational excellence</li><li>Ensuring full compliance with regulatory standards</li><li>Effectively maintaining study documentation and adhering to GCP frameworks</li></ul><h3>What We’re Looking For</h3><ul><li>Life sciences degree (or equivalent experience)</li><li>Hands on experience in CRA role / clinical operations</li><li>Strong understanding of GCP E6 (R3) and regulatory frameworks, Clinical data collection and monitoring processes</li><li>Effective stakeholder management: you’ll be dealing with external sites & HCPs</li><li>Strong attention to detail, organisation skills and documentation discipline</li><li>Knowledge of Trial Master Files and Essential Records</li></ul></div>