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Associate Trial Master File Director
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Full-time
- The Associate Trial Master File Director exhibits advanced experience with Project Management, is accountable for the oversight of projects for TMF Management, and ensures that projects are assigned realistic timelines with appropriate resources.
- This role oversees TMF technology and systems and works directly with the staff responsible for processing, assessing quality, and archiving of clinical trial documents from both external and internal sources, while fostering a culture of continuous improvement.
- Manages the Veeva roadmap by working closely with internal stakeholders and Veeva on the integration of other Veeva Platforms: RIMs, CTMS, QMS with eTMF to ensure it meets business needs.
- Designs and implements RPA technology within TMF Management to streamline TMF processes and improving efficiencies utlizing Bot technology.
- Represents TMF Management for all Veeva releases and enhancements.
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