Location: On-site, Peterborough
Employment Type: Full-time
Overview
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
Desirable
* Previous experience as a Clinical Research Coordinator or Research Nurse
* Experience working across multiple studies or therapeutic areas