Director of Submission Excellence

1 week ago


San Diego, California, United States ORIC Pharmaceuticals Full time
Key Responsibilities

This leadership role requires strong leadership and management skills, with the ability to inspire, motivate, and mentor teams. The Director/Associate Director will partner closely with regulatory affairs, clinical development, quality assurance, and manufacturing teams to ensure alignment on timelines, resources, and requirements for late-stage regulatory submissions and market approvals. They will also stay current with evolving global regulatory requirements and guidance documents.



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