Associate Director, Global Regulatory Lead, Oncology
Takeda Pharmaceutical Company(3 months ago)
About this role
The Associate Director, Global Regulatory Lead Oncology at Takeda defines and leads global regulatory strategies for oncology programs, overseeing major submissions and acting as primary FDA contact for assigned projects. The role coordinates cross-functional and regional teams to ensure global regulatory compliance and advance oncology candidates toward approval. It contributes to regulatory planning, stakeholder communication, and strategic decision-making across the development lifecycle.
Required Skills
- Regulatory Strategy
- Regulatory Submissions
- FDA Interactions
- Cross-Functional Collaboration
- Leadership
- Communication
- Negotiation
- Project Management
- Drug Development
Qualifications
- Bachelor's Degree in Scientific Discipline
- Advanced Degree in Scientific Discipline (Preferred)
About Takeda Pharmaceutical Company
takeda.comTakeda is a patient-focused, R&D-driven global biopharmaceutical company committed to bringing Better Health and a Brighter Future.
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