Associate Director, Regulatory Affairs CMC
Olema Oncology(20 days ago)
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.
Required Skills
- CMC Regulatory Expertise
- Clinical Research
- Oncology Knowledge
- Cross-Functional Collaboration
- Regulatory Submissions
Qualifications
- Bachelor's Degree in Scientific Field
- Advanced Degree
About Olema Oncology
olema.comOlema 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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