Clinical Research Coordinator

Discover International; Park Central; On-site; GBP 28,000 - 36,000; Full time

Job summary

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

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

Qualifications

• Experience coordinating multi-site clinical trials.
• Familiarity with ICH-GCP guidelines.
• Ability to manage trial documentation and timelines.
• Strong communication with sites and sponsors.
• Proficient in data handling and query resolution.

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/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

Trial coordination

ICH-GCP

Site management

MS Office

Education

Bachelor's degree in life sciences

Tools

TMF software

MS Office

Job description

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

Key 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