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-LjbffrDirector, Regulatory Submissions Lead — Cross-Functional PM in thousand oaks at Unknown Company
This position is listed as full time and onsite.