Clinical Research Coordinator

Job description

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

Extra information

Status

Open

Education Level

Secondary School

Location

Peterborough

Type of Contract

Full-time jobs

Published at

21-01-2026

Profession type

Health / Medical

Full UK/EU driving license preferred

No

Car Preferred

No

Must be eligible to work in the EU

No

Cover Letter Required

No

Languages

English