Clinical Research Coordinator

Discover International; West of England; On-site; GBP 30,000 - 42,000; Full time

Job summary

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

You will coordinate site start-up, maintain TMF per ICH-GCP, liaise with sites, sponsors and internal teams, support site visit scheduling and patient recruitment, prepare study materials, and help ensure data queries are resolved and audits are ready.

Qualifications

• Experience coordinating clinical trials per ICH-GCP guidelines.
• Familiarity with Trial Master Files (TMF) and site start-up.
• Ability to liaise with investigator sites, sponsors and internal teams to hit milestones.
• Experience in data query resolution and audit readiness.

Responsibilities

• Coordinate site start-up and maintain 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.

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