Senior Oncology Regulatory Affairs Lead
Listed on 2026-10-13
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Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
ORIC Pharmaceuticals is seeking a Regulatory Affairs professional to advance oncology product development. You will collaborate with regulatory operations, quality, CMC, nonclinical and clinical teams to support submissions, develop timelines, and ensure compliant, high-quality filings.
The role emphasizes proactive cross-functional work, regulatory intelligence, and strong writing/editing abilities, with a focus on global regulations and fast execution in a dynamic environment.
The Senior Oncology Regulatory Affairs Lead role at ORIC Pharmaceuticals is now open for applications in San Diego, CA, United States.
All applications are reviewed carefully by our team.
The position is based in San Diego, CA, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 145..
We aim to respond to suitable candidates as soon as possible.
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