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Job description
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.
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Worksite address
thousand oaks, CA, 91362, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.