Hybrid Clinical Trial Administrator - Oncology Trials

Fortrea; Maidenhead; Híbrido; GBP 30 000 - 42 000; Tempo integral

Resumo da oferta

Fortrea is seeking a pro-active Clinical Trial Administrator to join our London team. The role is office-based in central London for at least 3 days a week, with the remaining time home-based, to support complex oncological trials.

You will coordinate study activities, maintain TMF, support site material preparation, coordinate meetings, and liaise with vendors to ensure regulatory compliance and timely data production.

Qualificações

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

Responsabilidades

• 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

Conhecimentos

Project coordination

Documentation control

TMF management

Vendor liaison

Meeting support

Descrição da oferta de emprego

Fortrea is seeking a pro-active Clinical Trial Administrator to join our London team. The role is office-based in central London for at least 3 days a week, with the remaining time home-based, to support complex oncological trials.

You will coordinate study activities, maintain TMF, support site material preparation, coordinate meetings, and liaise with vendors to ensure regulatory compliance and timely data production.