Clinical Research Coordinator

Green Life Science; Cambridge; On-site; GBP 30,000 - 42,000; Full time

Job summary

Green Life Science in Cambridge is seeking a Clinical Research Coordinator to join a growing UK site network. You will coordinate day-to-day trial delivery in line with protocol, ICH-GCP and SOPs, and support participant visits at the Cambridge site.

You'll work closely with Investigators, sponsors and CROs, manage documentation, screens and enrolment, and help prepare for monitoring visits and audits. UK-based CRC experience is preferred.

Qualifications

• Previous CRC or research site experience (UK-based preferred).
• Sound working knowledge of ICH-GCP.
• Strong organisation, attention to detail and a patient-focused approach.
• Phlebotomy or clinical background is a plus.

Responsibilities

• Coordinate day-to-day delivery of clinical trials in line with protocol, ICH-GCP and SOPs
• Screen, consent, enrol and schedule participants, and support them through their study visits
• Manage source documentation, CRF/EDC entry and query resolution
• Prepare for and support monitoring visits, audits and inspections
• Work closely with Investigators, sponsors and CROs

Skills

Research site exp

ICH-GCP knowledge

Organisational skills

Patient focus

Phlebotomy

Job description

Clinical Research Coordinator (CRC) – Cambridge

We’re partnering with a new UK clinical research site network, founded by a leadership team with 40+ years of combined site experience, to hire a Clinical Research Coordinator for their Cambridge site.

This is a chance to join a growing organisation early, help shape how the site runs, and work across a varied portfolio of studies.

The role

• Coordinate day-to-day delivery of clinical trials in line with protocol, ICH-GCP and SOPs
• Screen, consent, enrol and schedule participants, and support them through their study visits
• Manage source documentation, CRF/EDC entry and query resolution
• Prepare for and support monitoring visits, audits and inspections
• Work closely with Investigators, sponsors and CROs

What you’ll bring

• Previous CRC or research site experience (UK-based preferred)
• Sound working knowledge of ICH-GCP
• Strong organisation, attention to detail and a patient-focused approach
• Phlebotomy or clinical background is a plus