or apply directly on Olema Oncology's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 49 days Olema Oncology's roles stay open a median of 50 days
- Reposted
- No
- Salary listed
- No 71% of Olema Oncology's roles list one
- Ghost-job risk at Olema Oncology
- high 11 stale, 0 reposted of 21 open
- Hiring momentum
- 31 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-24
Measured from postings appearing on and disappearing from Olema Oncology's own greenhouse board since 2026-08-03. Full hiring picture for Olema Oncology.
About this role
The Senior Director, EU Regulatory Affairs at Olema Oncology will lead the Regulatory Affairs function for the company's European subsidiary, focusing on oncology programs and commercialization efforts. Responsibilities include developing and executing EU regulatory strategies, managing interactions with regulatory authorities, overseeing Clinical Trial Applications and Marketing Authorization Applications, and ensuring compliance with EU regulations. The role requires strategic leadership and collaboration with cross-functional teams to support business objectives and regulatory governance.
- benefits
- 1/5
- freshness
- 1/5
- career value
- 5/5
- role clarity
- 5/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Olema Oncology as an employer.
What you need
- Advanced degree in Life Sciences, Pharmacy, Regulatory Science, or a related scientific discipline; advanced professional degree preferred
- Minimum of 15 years of progressive Regulatory Affairs experience within the biotechnology or pharmaceutical industry
- 5+ years of direct leadership
- Effective communicator with executive presence and influencing skills
- Sound judgment and decision-making in complex, risk-based environments
- Demonstrated expertise in European regulatory affairs, including the EU Clinical Trials Regulation (CTR), CTIS, EMA centralized procedures, and interactions with National Competent Authorities
Nice to have
- Oncology regulatory experience is strongly preferred
Worth weighing
- No specific salary or benefits details provided in the posting
- The role requires 15% - 20% international travel
- The company is described as a small, nimble group which may imply a fast-paced work environment
Summarised from Olema Oncology's posting. Read the full original.
Listed by Olema Oncology on their greenhouse job board, last confirmed open on 2026-09-24. PitchMeAI is not the employer.
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