Multi-Site Clinical Research Coordinator: Trials & Data Integrity

Discover International; Aberdeen City; On-site; GBP 28,000 - 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 clinical trials across oncology, cardiovascular, and rare disease indications.

You will coordinate site start-up, maintain TMF per ICH-GCP, and liaise with investigator sites, sponsors and internal teams to meet trial milestones. You will assist CRAs with visit scheduling, data queries, and study trackers, ensuring audit readiness.

Qualifications

• Experience coordinating multi-site clinical trials.
• Familiarity with ICH-GCP standards.
• Ability to manage TMF and trial documentation.

Responsibilities

• Coordinate site start-up and maintain TMF per ICH-GCP.
• Liaise with investigator sites, sponsors and internal teams to hit milestones.
• Support CRAs with visit scheduling/reports and track recruitment.
• Prepare study materials and manage trackers.
• Help resolve data queries and ensure audit readiness.

Skills

Site coordination

ICH-GCP

Trial Master File (TMF)

Liaison with sites

Data queries

Job description

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

You will coordinate site start-up, maintain TMF per ICH-GCP, and liaise with investigator sites, sponsors and internal teams to meet trial milestones. You will assist CRAs with visit scheduling, data queries, and study trackers, ensuring audit readiness.