Clinical Research Coordinator — Multi-Site Trials

Discover International; Wolverhampton; On-site; GBP 28,000 - 38,000; Full time

Job summary

Discover International is partnered with a UK-based CRO seeking a Clinical Research Coordinator to support multi-site trials across oncology, cardiovascular, and rare disease indications. You will coordinate site start-up, maintain TMFs, liaise with sites and sponsors, and support CRAs with visits and recruitment tracking.

The role involves preparing study materials, managing trackers, and ensuring data queries are resolved with audit readiness in mind.

Qualifications

• Experience coordinating multi-site clinical trials in line with ICH-GCP.
• Strong attention to detail in study documentation and tracking.
• Excellent communication with investigators, sponsors and internal teams.

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.

Skills

Site coordination

Study documentation

Stakeholder communication

Data query resolution

Education

Bachelor's degree in life sciences

Tools

TMF Software

Job description

Discover International is partnered with a UK-based CRO seeking a Clinical Research Coordinator to support multi-site trials across oncology, cardiovascular, and rare disease indications. You will coordinate site start-up, maintain TMFs, liaise with sites and sponsors, and support CRAs with visits and recruitment tracking.

The role involves preparing study materials, managing trackers, and ensuring data queries are resolved with audit readiness in mind.