Clinical Trial Administrator, London

Fortrea; Maidenhead; Ibrido; GBP 24.000 - 32.000; Tempo pieno

Descrizione del lavoro

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.

Competenze

• 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.

Mansioni

• 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.

Conoscenze

Clinical Trial Admin

Regulatory Documentation

TMF Management

Vendor Liaison

Descrizione del lavoro

Fortrea is currently seeking a pro‑active Clinical Trial Administrator to join our expanding team in London. This client-dedicated role is office based in central London for at least 3 days a week with the rest of the time being spent working from home. Ideally you will have at least 1-2 years experience of supporting Clinical Trials in the UK. Much of the work will involve complex oncological clinical trials, providing valuable opportunities to develop your skills and expertise.

What You’ll Do

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

Requirements

• A minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company - this is essential!
• Must be within commuting distance of Central London (office-based 3 days per week)
• Basic understanding of biology and biological processes
• Good organizational and time management skills

This role is a full time & permanent position to be employed through Fortrea.

This is a great opportunity to gain hands‑on experience in clinical research and contribute to high-quality clinical data production. If you thrive in a fast-paced environment and enjoy working with a dynamic team, we’d love to hear from you!

Learn more about our EEO & Accommodations request here.