Clinical Research Coordinator

Discover International; Warrington; On-site; GBP 30,000 - 42,000; Full time

Job summary

Discover International, in partnership with a UK-based CRO, seeks a Clinical Research Coordinator to support multi-site trials across oncology, cardiovascular, and rare diseases. You will coordinate site start-up and maintain TMFs per ICH-GCP, while liaising with investigators, sponsors and internal teams to hit milestones.

You will assist CRAs with visit scheduling, data queries, consent forms, and study trackers, ensuring audit readiness and timely milestone progress.

Qualifications

• Experience coordinating multi-site clinical trials.
• Familiarity with ICH-GCP and regulatory requirements.
• Experience maintaining Trial Master Files (TMF).
• Strong communication with investigators, sponsors and internal teams.
• Ability to support data queries and audit readiness.

Responsibilities

• Coordinate site start-up activities and TMF maintenance per ICH-GCP.
• Liaise with investigator sites, sponsors, and internal teams to hit trial milestones.
• Support CRAs with visit scheduling, source data verification, and reports.
• Prepare study materials (consent forms, CRFs) and manage study trackers.
• Help resolve data queries and ensure audit/inspection readiness.

Skills

Site coordination

ICH-GCP knowledge

TMF management

Stakeholder liaison

Data query support

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