Clinical Research Coordinator

Discover International; Chester; On-site; GBP 28,000 - 45,000; Full time

Job summary

Discover International is partnered with a UK-based CRO seeking a Clinical Research Coordinator to support multi-site clinical trials across oncology, cardiovascular, and rare disease areas.

You will coordinate site start-up, maintain TMF per ICH-GCP, liaise with investigators and sponsors, and assist CRAs with scheduling and reporting. You’ll help prepare study materials and manage trackers while ensuring data quality and audit readiness.

Qualifications

• Experience coordinating multicenter clinical trials across sites.
• Knowledge of ICH-GCP guidelines and regulatory requirements.
• Strong organizational and communication skills for cross-functional teams.

Responsibilities

• Coordinate site start-up activities and maintain TMF per ICH-GCP.
• Liaise with investigator sites, sponsors, and internal teams to hit milestones.
• Support CRAs with scheduling, visit reports, and recruitment tracking.
• Prepare study materials (consents, CRFs) and manage trackers.
• Address data queries and ensure audit/inspection readiness.

Skills

ICH-GCP

Trial coordination

Data management

Stakeholder liaison

Education

Bachelor's in Life Sciences

Tools

TMF software

EDC systems

Job description

Discover International is partnered with a UK-based CRO who are seeking a Clinical Research Coordinator to support multi-site clinical trials across oncology, cardiovascular, and rare disease indications.

Key Responsibilities

• Coordinate site start-up and maintain Trial Master Files (TMF) per ICH-GCP
• Liaise with investigator sites, sponsors, and internal teams to hit trial milestones
• Support CRAs with visit scheduling/reports and track patient recruitment
• Prepare study materials (consent forms, CRFs) and manage study trackers
• Help resolve data queries and ensure audit/inspection readiness