Job Summary
A company is looking for a TMF Specialist.
Key Responsibilities
- Manage and maintain the Trial Master File (TMF) throughout the clinical trial lifecycle
- Ensure compliance with regulatory requirements and internal standards related to TMF documentation
- Coordinate with cross-functional teams to facilitate timely and accurate TMF submissions and updates
Required Qualifications
- Bachelor's degree in a relevant field
- Experience in clinical trial management or related areas
- Knowledge of regulatory guidelines for TMF management
- Familiarity with electronic TMF systems
- Ability to work independently and collaboratively in a remote environment
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