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Director, Regulatory Affairs Strategy – Oncology
RegeneronDirector of Regulatory Affairs at Regeneron leading global regulatory activities for oncology products. Overseeing clinical submissions and strategic regulatory planning while ensuring compliance with regulations.
Posted 5/20/2026full-timeWarren • Massachusetts, New Jersey, New York • 🇺🇸 United StatesLead💰 $205,000 - $341,600 per yearWebsite
About the role
Key responsibilities & impact- Provide leadership on global regulatory activities for the assigned products.
- Focus on Clinical Regulatory filings and provide regulatory leadership on project teams.
- Supply, lead and/or supervise IND/CTA and BLA submissions activities.
- Provide interpretation of regulatory authorities’ feedback, policies and guidelines.
- Lead the development of regulatory strategic plans in conjunction with project teams or through your reports.
- Own the preparation of major clinical submissions required for regulatory approval.
- Work with project teams to resolve complex project issues.
- Utilize regulatory expertise and knowledge of regulatory requirements and regulations to interpret, plan, and communicate requirements.
- Assure compliance with regulations and project team timelines.
- Provide interpersonal support and lead personnel.
Requirements
What you’ll need- MD, Ph.D. or Pharm D. degree
- minimum of 10 years of pharmaceutical industry experience
- at least 7 years of regulatory experience
- strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices
- strong interpersonal skills both written and verbally
- high attention to detail; ability to coordinate and prioritize assigned projects according to company goals
- interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred
Benefits
Comp & perks- health and wellness programs (including medical, dental, vision, life, and disability insurance)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental leave) for eligible employees at all levels!
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
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Hard Skills & Tools
IND submissionsCTA submissionsBLA submissionsregulatory strategic planningregulatory complianceclinical submissions preparationregulatory interpretationdrug development processproject management
Soft Skills
leadershipinterpersonal skillscommunication skillsattention to detailcoordinationprioritization
Certifications
MDPh.D.Pharm D.