Job Description
Location: South West Region UK
Make an impact on global health by driving high-quality clinical research. In this role, you’ll be the primary site contact and operational lead across all phases of clinical trials—ensuring excellence in performance, compliance, and patient safety. Under the guidance of the CRA Manager, you’ll own your sites end-to-end, build strong relationships, and help expand our clinical footprint while upholding ICH/GCP and local regulatory standards, our organization’s policies and procedures, quality standards, and adverse event reporting requirements.
What you’ll do
1. Be the primary site contact and site manager throughout the study lifecycle, taking overall accountability for assigned sites
2. Build, nurture, and maintain strong site relationships to ensure stable performance from start-up through close-out
3. Perform remote and on-site monitoring in accordance with ICH-GCP, local regulations, protocol, monitoring plans, and our organization’s SOPs
4. Ensure high-quality data: complete, accurate, unbiased—and always with participant rights, safety, and well-being protected
5. Conduct all site visit types (validation, initiation, monitoring, close-out), with timely, clear, and comprehensive reporting
6. Drive site readiness: coordinate cross-functional activities and c...