Posted 30 April, 2026
Job Id: 627623
Clinical and Health – Dir Reg Affairs
Job Description
Provides senior regulatory leadership and strategic guidance to support late-stage clinical development programs, ensuring alignment with global regulatory requirements. Acts as the primary regulatory lead for a fast-paced biotech environment, partnering cross-functionally to drive regulatory strategy through Phase III and preparation for potential registration.
Key Responsibilities:
- Lead global regulatory strategy for Phase III clinical programs, with a focus on vaccines
- Provide hands-on leadership for regulatory submissions and interactions (e.g., FDA, EMA), including NDA/BLA readiness where applicable
- Serve as interim Regulatory Affairs Lead, ensuring continuity of ongoing programs and regulatory commitments
- Advise internal stakeholders on evolving regulatory requirements and risk mitigation strategies
- Support preparation, review, and delivery of high-quality regulatory documents and submissions
- Act as key liaison with clinical, CMC, and executive teams in a high-pressure, fast-moving biotech setting
Qualifications:
- Extensive Regulatory Affairs experience (typically 12-15+ years) in biotech/pharma
- Proven experience leading global regulatory strategy for Phase III clinical programs
- Vaccine experience strongly preferred
- Prior experience with NDA/BLA submissions or late-stage regulatory interactions is a plus
- Demonstrated ability to operate effectively in fast-paced, high-pressure environments
- Strong leadership, communication, and stakeholder management skills
Pay Rate Range: $70-117/hr depending on experience
Equal Opportunity Employer
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