Global Regulatory Lead, Oncology — Strategy & Submissions
USA - 3316 Takeda Development Center Americas, Inc.
Takeda is seeking a Director, Global Regulatory Lead Oncology to set global regulatory strategy and lead major submissions for high-impact oncology programs. You will serve as GRL on GPTs, coordinate with global teams, and ensure FDA submissions and other major filings are executed on time with high quality. The role requires 8+ years in pharma regulatory affairs, strong FDA knowledge, and ability to influence across global teams. #J-18808-Ljbffr USA - 3316 Takeda Development Center Americas, Inc.
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