We are supporting a growing clinical research site network seeking a Clinical Research Coordinator to support the day-to-day delivery of clinical trials at our Peterborough site. This is a hands-on, on-site role working closely with investigators, patients, and sponsors to ensure studies are run to GCP and protocol.
Key Responsibilities
- Coordinate and support clinical trials from start-up to close-out
- Screen, recruit, and schedule study participants
- Conduct study visits and collect trial data in line with protocol
- Maintain accurate study documentation and trial master files
- Liaise with investigators, sponsors, CROs, and monitors
- Ensure compliance with GCP, SOPs, and regulatory requirements
- Support monitoring visits, audits, and inspections
Requirements
- Experience working in clinical research (site-level experience preferred)
- Good understanding of GCP and clinical trial processes
- Strong organisational and communication skills
- Comfortable working on-site in a fast-growing environment
- Previous experience as a Clinical Research Coordinator or Research Nurse
- Experience working across multiple studies or therapeutic areas
