Clinical Research Coordinator

Discover International; Wakefield; On-site; GBP 32,000 - 42,000; Full time

Job summary

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

You will coordinate site start-up and maintain TMF per ICH-GCP, liaise with investigator sites, sponsors and internal teams to hit milestones, support CRAs with visits and reports, prepare study materials, and manage study trackers. Ensure audit readiness and data query resolution.

Qualifications

• Experience with ICH-GCP and trial master files (TMF).
• Ability to coordinate multi-site startup activities and milestones.
• Strong collaboration with investigators, sponsors and internal teams.

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 patient recruitment tracking.
• Prepare study materials (consent forms, CRFs) and manage trackers.
• Help resolve data queries and ensure audit/inspection readiness.

Skills

Site coordination

TMF management

Stakeholder liaison

CRF preparation

Audit 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