Clinical Research Coordinator

Green Life Science; Peterborough; On-site; GBP 30,000 - 45,000; Full time

Job summary

A clinical research organization in Peterborough is seeking a Clinical Research Coordinator to oversee clinical trials. This role involves coordinating trials from start to finish, recruiting participants, and ensuring compliance with GCP and other regulations. Ideal candidates will have previous experience in clinical research, strong organizational skills, and the ability to work effectively in a dynamic environment. Join a growing team focused on delivering results in 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.
• 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.

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.

Skills

Organisational skills

Communication skills

Understanding of GCP

Job description

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