Hybrid Clinical Trial Administrator – London

Fortrea; Maidenhead; Hybrid; GBP 24,000 - 32,000; Full time

Job summary

Fortrea in London is seeking a proactive Clinical Trial Administrator to join our growing team. This client-dedicated role is office-based in central London for at least 3 days a week, with the remainder of time spent working from home.

Ideally you will have 1–2 years of experience supporting Clinical Trials in the UK, especially in oncology trials. You will coordinate project teams, maintain regulatory documentation, assist with site materials, and manage TMF records.

Qualifications

• 12+ months of Clinical Research Admin experience in CRO or pharma required.
• Familiarity with regulatory documentation and TMF processes.
• Strong organizational and time-management skills.

Responsibilities

• Communicate with project teams and track study activities.
• Maintain essential documentation and regulatory compliance.
• Support site and study material preparation.
• Assist with meeting coordination and minute-taking.
• Manage Trial Master File (TMF) documentation and quality control.
• Liaise with vendors and coordinate study supply shipments.
• Provide general administrative and systems support.

Skills

Clinical Trial Admin

Regulatory Documentation

TMF Management

Vendor Liaison

Job description

Fortrea in London is seeking a proactive Clinical Trial Administrator to join our growing team. This client-dedicated role is office-based in central London for at least 3 days a week, with the remainder of time spent working from home.

Ideally you will have 1–2 years of experience supporting Clinical Trials in the UK, especially in oncology trials. You will coordinate project teams, maintain regulatory documentation, assist with site materials, and manage TMF records.