Tmf specialist
Lo cation: This position may be performed remotely but requires flexibility and willingness to travel as needed.
Position Summary We are looking for a TMF Specialist to help organize, review, and maintain essential clinical trial documents in our electronic Trial Master File (eTMF) system. This role ensures our records meet quality standards and regulatory guidelines. Key Responsibilities- Review and quality check trial documents to ensure accuracy and compliance.
- File and maintain essential records in the eTMF system.
- Flag and track quality issues, ensuring they are resolved quickly.
- Support filing and archiving across multiple clinical studies.
- Work closely with TMF Operations Lead to update filing processes and guidelines.
- Help manage periods of high document submission.
- Bachelor’s degree or equivalent.
- 2-4 years of experience in clinical trials, TMF, or related roles (Sponsor, CRO, or Site).
- Knowledge of ICH-GCP, good documentation practices, and eTMF systems (e.g., Veeva).
- Organized and detail oriented
- Great communicator and team player
- The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
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