Dyne Therapeutics is seeking an Associate Director, Trial Master File (TMF) Lead to develop and drive the global TMF strategy and governance. You will ensure end-to-end TMF oversight across the clinical portfolio, partnering with Clinical Operations, Quality, Regulatory, and CROs to support inspection readiness and compliant operations.
The role emphasizes enterprise TMF processes, KPIs, and proactive risk management to sustain high-quality clinical execution at scale.
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