CRA II: Lead Site Monitoring & Regulatory Compliance

A clinical research organization in the United Kingdom is seeking an experienced CRA II to act as the primary contact for trial sites. You will ensure high standards of compliance and documentation across multi-centre studies while building strong relationships with site staff. The ideal candidate will have 2–3+ years of clinical monitoring experience and strong knowledge of ICH-GCP. This is a full-time position. #J-18808-Ljbffr