Clinical Research Coordinator

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

Job summary

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

You will coordinate site start-up, maintain TMF per ICH-GCP, liaise with sites, sponsors and internal teams, support CRAs with visit scheduling and data tracking, and help prepare study materials while ensuring audit readiness.

Qualifications

• Experience coordinating multi-site clinical trials.
• Familiar with ICH-GCP and trial master files.
• Ability to liaise with investigators and sponsors.
• Strong organizational and communication skills.

Responsibilities

• Coordinate site start-up and maintain TMF per ICH-GCP.
• Liaise with investigator sites, sponsors, and internal teams to meet trial milestones.
• Support CRAs with visit scheduling, reports, and patient recruitment tracking.
• Prepare study materials (consent forms, CRFs) and manage trackers.
• Help resolve data queries and ensure audit/inspection readiness.

Skills

Site coordination

ICH-GCP knowledge

TMF management

Sponsor/investigator liaison

Data query resolution

Education

Bachelor's degree in life sciences

GCP certification

Tools

TMF systems

CRF knowledge

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