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The TMF Coordinator is responsible for maintaining the quality, completeness, and compliance of Trial Master File documentation in accordance with global regulatory standards. They will perform document QC, resolve filing discrepancies, and collaborate with cross-functional teams to ensure inspection readiness.
We are seeking a detail-oriented and highly organized TMF Coordinator to join our TMF Operations team. In this role, you will be responsible for maintaining the quality, completeness, and compliance of Trial Master File (TMF) documentation in alignment with global regulatory requirements and company standards. You will play a key role in ensuring that TMF content remains inspection-ready and supports clinical trial execution through effective document management and collaboration with cross-functional stakeholders.
Positions Available: 2; Note this position is cross-listed in multiple countries.
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