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TMF Study Owner

United States   •  Negotiable  •  Permanent, Full time

Senior Clinical Trial Administrator
Home based - United States

Company role overview;

This world renowned TMF specialist organisation is currently looking for a TMF Administrator to join a rapidly growing and dynamic team. You will have the opportunity to work on a unique combination of eTMF technologies and utilise your skillset. The ideal candidate will have a good understanding of the Trial Master File (TMF) and essential document recognition skills.

Main Responsibilities;

- Remap of TMF documentation
- Audit/ Review TMF and ISF documentation
- Set up and maintenance of eTMF to meet client needs
- Monitor the completeness and quality of TMF content
- Devising new filing structures as well as basic filing maintenance
- Subsidiary file management
- Support external Study Teams in the effective management of TMF

Candidate Requirements;

- 3+ years Clinical Operations or TMF oversight
- Demonstrated awareness of sponsor oversight
- Experience and knowledge of ICH/GCP documentation requirements
- Outstanding verbal and written communications skills

If you would like to hear more about this role please contact Jessica Wheeler at Clinical Professionals at jessica@clinicalprofessionals.co.uk.

  • Agency: Cpl Life Sciences
  • Contact: Jessica Wheeler
  • Reference: JO-2006-450694
  • Updated: 16th July 2021
  • Expires: 13th August 2021

Cpl Life Sciences

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