Associate Director, Clinical Trial Delivery and Pharmacovigilance Documentation Excellence

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Job Description

OBJECTIVES/PURPOSE:

• Build, lead, and scale Takeda's Clinical & PV Document Excellence Global Capability Center (GCC) as a strategic capability supporting Clinical Development and Pharmacovigilance records managment and inspection readiness globally.

• Provide operational leadership for sponsor-owned TMF operations, quality review services, document processing, inspection readiness support, records stewardship activities, and continuous improvement initiatives.