Clinical Research Coordinator – Peterborough, England, UK Clinical Research Site Network

Greenlsr; Peterborough; On-site; GBP 60,000 - 80,000; Full time

Job summary

A clinical research organization in Peterborough is seeking a Clinical Research Coordinator to oversee clinical trials. This hands-on, on-site role involves coordinating studies, recruiting participants, and ensuring compliance with GCP and protocol. The ideal candidate should have experience in clinical research and strong organizational skills. The position offers a full-time opportunity to work in a dynamic environment, contributing to the advancement of clinical research.

Qualifications

• Experience working in clinical research, preferably at the site-level.
• Good understanding of GCP and clinical trial processes.
• Strong organisational and communication skills.

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.

Skills

Clinical research experience

Organisational skills

Communication skills

Understanding of GCP

Job description

Peterborough, England, United Kingdom

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

How To Apply

Send your resume and cover letter to: [e-mail]

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