Clinical Research Coordinator

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