Olema Oncology

Associate Director, Regulatory Affairs CMC

Olema Oncology(20 days ago)

California, San Francisco, CAOnsiteFull TimeManager$190,000 - $205,000Regulatory Affairs
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About this role

As the Associate Director, Regulatory Affairs CMC at Olema Oncology, you will develop and execute CMC regulatory strategies for product development and post-approval, ensuring alignment with global Health Authority requirements. The role involves collaborating with cross-functional teams to provide guidance on high-quality regulatory submissions and strategies, contributing to the organization’s mission of improving therapies for breast cancer and beyond.

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Required Skills

  • CMC Regulatory Expertise
  • Clinical Research
  • Oncology Knowledge
  • Cross-Functional Collaboration
  • Regulatory Submissions

Qualifications

  • Bachelor's Degree in Scientific Field
  • Advanced Degree
Olema Oncology

About Olema Oncology

olema.com

Olema Oncology is a cancer medicines company focused on innovating therapies for breast cancer and other endocrine-driven tumors. The company is rapidly advancing a pipeline of drug candidates designed to target the biology of endocrine-driven disease. Olema’s work centers on translating cutting‑edge science into treatments that meaningfully impact patients, progressing programs toward clinical evaluation.

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