Senior Clinical Trial Associate
Job Description
Senior Clinical Research Associate | London, UK | 6-Month Contract (Full-time) HYBRID
Key responsibilities
- Support the day-to-day operational delivery of Phase I–III clinical trials across multiple complex indications
- Maintain and oversee Trial Master File (TMF) quality and completeness to ensure inspection readiness
- Assist with study start-up activities including site documentation collection, regulatory submissions and site activation support
- Coordinate trial documentation, vendor communications and study tracking to support global clinical operations teams
- Collaborate with Clinical Trial Managers, CRAs, regulatory teams and external partners to ensure timely study execution
- Track study milestones, manage essential documents and support reporting across clinical programs
- Assist with preparation and management of study materials including investigator meeting documentation and training materials
- Support audit and inspection readiness activities and ensure compliance with ICH-GCP and internal procedures
Candidate requirements
- Minimum 5 years’ experience as a Clinical Trial Associate or within a comparable clinical operations role
- Strong experience supporting Phase I–III clinical trials
- Experience working within biotechnology environments, ideally supporting innovative or complex therapeutic programs such as cell or gene therapy
- Exposure to multiple complex therapeutic areas and global clinical trial operations
- Strong understanding of clinical trial documentation, TMF management and regulatory processes
- Excellent organisational skills with the ability to manage multiple studies and priorities simultaneously
- Strong communication skills and ability to work effectively within cross-functional clinical teams
What is offered
- Opportunity to work within an innovative cell therapy biotech environment
- Exposure to cutting-edge clinical development programs
- Hybrid working model in London
- 6-month fixed term contract.
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