Director, Regulatory Submissions Lead — Cross-Functional PM
Kite Pharma
Kite Pharma seeks a Director of Submission Project Management to lead strategic planning and execution of major regulatory submissions globally. You will coordinate clinical data readiness, cross-functional teams, and governance to ensure timely, compliant filings. Prerequisites include a doctorate, extensive regulatory expertise, and strong leadership across Development, Regulatory, and Quality functions. Bay Area base with competitive compensation and broad benefits. #J-18808-Ljbffr Kite Pharma
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...this vital role the Executive Director, US Brand Lead for ABP 206 & ABP 234 is... ...and ensure every commercial function is prepared to deliver... ...and patient outcomes upon regulatory approval. As a member of the... ..., executive reporting, and cross-functional performance reviews...WorldwideFlexible hours
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