Senior Clinical Research Associate | London, UK | 6-Month Contract (Full-time)
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 contract.