Clinical Research Coordinator — Multi-Site Trials

Discover International; West Alvington; On-site; GBP 28,000 - 38,000; 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, manage TMF per ICH-GCP, and liaise with investigator sites, sponsors, and internal teams to hit trial milestones.

You will assist CRAs with visit scheduling and reports, prepare study materials such as consent forms and CRFs, track patient recruitment, and help resolve data queries to

Qualifications

• Coordination of multi-site clinical trials and regulatory tasks.
• Experience with ICH-GCP and TMF processes.
• Strong communication with sites, sponsors and internal teams.
• Knowledge of trial milestones and data management in research.

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

Skills

Trial coordination

GCP/ICH

Regulatory documentation

Clinical trials

Job description

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, manage TMF per ICH-GCP, and liaise with investigator sites, sponsors, and internal teams to hit trial milestones.

You will assist CRAs with visit scheduling and reports, prepare study materials such as consent forms and CRFs, track patient recruitment, and help resolve data queries to