Clinical Research Coordinator – Multi-Site Trials

Discover International; Basildon; On-site; GBP 28,000 - 40,000; Full time

Job summary

Discover International partners with a UK-based CRO to recruit a Clinical Research Coordinator to support multi-site clinical trials across oncology, cardiovascular, and rare disease areas. The role involves coordinating site start-up, maintaining TMF per ICH-GCP, and liaising with investigator sites, sponsors, and internal teams to achieve trial milestones.

You will support CRAs with visit scheduling and reporting, prepare study materials, manage trackers, and help resolve data queries to

Qualifications

• Experience coordinating multi-site clinical trials.
• Familiarity with Trial Master Files (TMF) and ICH-GCP guidelines.
• Ability to liaise with investigator sites, 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 milestones.
• Support CRAs with visit scheduling and reports, track recruitment.
• Prepare study materials (consent forms, CRFs) and manage trackers.
• Help resolve data queries and ensure audit readiness.

Skills

Site coordination

Stakeholder liaison

Visit scheduling

Documentation management

Data query resolution

Tools

TMF management

ICH-GCP familiarity

Job description

Discover International partners with a UK-based CRO to recruit a Clinical Research Coordinator to support multi-site clinical trials across oncology, cardiovascular, and rare disease areas. The role involves coordinating site start-up, maintaining TMF per ICH-GCP, and liaising with investigator sites, sponsors, and internal teams to achieve trial milestones.

You will support CRAs with visit scheduling and reporting, prepare study materials, manage trackers, and help resolve data queries to