**West Coast Candidates**
Job opportunity with a top biopharmaceutical company that is looking for a TMF Administrator to join their team on a 6-12 month contract with a possibility for conversion or extension!
Pay Rate: Open
Qualifications:
- Bachelor's Degree preferred
- 3+ years' experience managing or supporting TMF actives for clinical trials
- Experience in managing TMF documents during regulatory inspections
- Ability to multi-task and manage several projects in parallel while paying attention to detail
- Strong critical thinking skills and ability to contribute creative yet practical solutions to problems
Job Description/Skills:
- Setting up our TMF according to the TMF plan and training contributors on the system and document requirements
- Participate in the Quality Control of documents (paper and electronic) submitted to the TMF
- Facilitate the review and submission of TMF records as well a completing the archival process
- Support the coordination of the transfer of study-specific trial master files from the CRO
- Maintain awareness of study events and the associated documentation requirements through collaboration with Study Team
Benefits/Perks:
- 401k
- Health Insurance
Please apply here directly if interested but If you are genuinely not interested, is there someone you can recommend?