Remotely
team leadershiponcologyregulatory affairsglobal regulatory strategyregulatory submissions
Job Description
📋 Description
- Lead Global Regulatory Teams for late-stage oncology programs with global complexity.
- Develop and execute global regulatory strategies for development, registration, labeling, and
- Represent Regulatory Affairs on product teams and governance bodies to influence decisions.
- Develop Global Regulatory Strategic Plans with cross-functional input.
- Identify and mitigate regulatory risks across development and commercialization.
- Lead global regulatory submissions and ensure consistency with strategy.
🎯 Requirements
- Doctorate with 5+ years regulatory biotech experience or Master’s with 9+ years or Bachelor’s with
- 5+ years of direct people leadership/management experience.
- Experience leading regulatory strategy for highly complex late-stage programs.
- Oncology regulatory experience strongly preferred.
- Proven success in regulatory submissions and agency interactions.
- Strong communication, leadership, and cross-functional collaboration skills.
🎁 Benefits
- Annual U.S. base salary range of $215,204.70–$291,159.30, determined by skills/experience.
- Comprehensive health and welfare benefits, including medical, dental, vision.
- Retirement plan with company contributions; life and disability insurance.
- Flexible spending accounts and discretionary bonus.
- Stock-based long-term incentives and paid time-off programs.
- Career development and inclusive, collaborative culture.
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