Trial Master File Document Coordinator
Cancer Research UK(1 month ago)
About this role
The Trial Master File Document Coordinator will support the Centre for Drug Development by leading TMF activities and maintaining an inspection-ready eTMF for early-phase oncology studies. This fixed-term role works on the DETERMINE precision medicine trial and sits within the Clinical Study Coordinator team, reporting to the Clinical Operations Manager. The post is based in Stratford, London and contributes to regulatory-compliant document management to accelerate cancer drug development.
Required Skills
- Document Management
- TMF
- eTMF
- Veeva Vault
- ICH GCP
- Attention To Detail
- Microsoft Office
- Organisational Skills
- Quality Checks
- Problem Solving
+2 more
About Cancer Research UK
cancerresearchuk.orgWe are the world’s leading independent cancer charity dedicated to saving lives through research, influence and information.
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