Clinical Research Coordinator – Multi-Site Trials & TMF

Discover International; Birmingham; On-site; GBP 30,000 - 38,000; Full time

Job summary

Discover International is partnered with a UK-based CRO to recruit a Clinical Research Coordinator to support multi-site trials across oncology, cardiovascular, and rare disease areas. You will coordinate site start-up, maintain trial master files, liaise with sites, sponsors and internal teams, and assist with data queries and recruitment.

You will help ensure regulatory compliance, assist with audit readiness, and contribute to study documentation and trackers in a dynamic clinical research

Qualifications

• Minimum degree in life sciences, healthcare, or related field.
• Experience coordinating clinical trials or research studies is preferred.
• Familiarity with TMF, ICH-GCP, and regulatory requirements is desirable.

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 patient recruitment.
• Prepare study materials (consent forms, CRFs) and manage trackers.
• Resolve data queries and support audit/inspection readiness.

Skills

Site coordination

TMF management

ICH-GCP knowledge

Stakeholder liaison

Education

Bachelor's degree in life sciences/healthcare

Tools

E-clinical systems

Microsoft Excel

Job description

Discover International is partnered with a UK-based CRO to recruit a Clinical Research Coordinator to support multi-site trials across oncology, cardiovascular, and rare disease areas. You will coordinate site start-up, maintain trial master files, liaise with sites, sponsors and internal teams, and assist with data queries and recruitment.

You will help ensure regulatory compliance, assist with audit readiness, and contribute to study documentation and trackers in a dynamic clinical research