Global Regulatory Strategist

Job title: Global Regulatory Strategist

• Grade: L3

• Location: Morristown, NJ

About the job

Our team is involved in developing regulatory product strategies for the oncology therapeutic area, leading regulatory efforts in the development stage of drug products. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless

opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

The Regulatory Strategist provides regulatory expertise and guidance on procedural and documentation requirements to GRT and cross-functional teams working flexibly within and across regions to ensure delivery of business objectives.

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

About Sanofi

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

Cross - Functional Collaboration:

• Enables the Global Regulatory Lead (GRL) by providing quality regulatory input and positioning to internal business partners, including clinical development teams, commercial teams, and the Global Regulatory Team (GRT) for assigned projects
• Liaises with nonclinical, clinical, CMC, commercial, and other internal business partners in partnership with the GRL to enable successful regulatory outcomes
• Contributes to a harmonized, One Sanofi regulatory voice through participation in appropriate committees and forums, at the direction of the GRL
• Proactively contributes to the GRT with curiosity and openness to diverse perspectives, providing strategic input on the Target Product Profile (TPP), business planning, governance, and committees; may be requested to lead GRT meetings

Health Authority (HA) Engagement:

• Accountable for developing HA engagement and interaction plans for assigned products, including: (1) authoring briefing documents focused on strategy and scientific content and leading team meeting preparations
• May lead HA meetings and preparations as designated
• May serve as regional/local regulatory lead and point of contact with Health Authorities for projects/products within remit, as needed

Regulatory Submissions & Operations:

• Leads submission teams or regulatory sub-teams to ensure timely filings that meet product launch deadlines for:
  • Marketing applications: NDA/BLA/MAA/Extensions
  • Clinical trial applications: IND/CTA/CTR submissions aligned with trial initiation milestones
• Responsible for developing and maintaining the core global dossier; collaborating with regional leads on region-specific submissions
• Leads development and implementation of expedited regulatory pathways, including:
  • Development programs: Fast Track Designation (FTD), Breakthrough Therapy Designation (BTD), Regenerative Medicine Advanced Therapy (RMAT), PRIME
  • Review processes: Priority Review, Project Orbis, Real-Time Oncology Review (RTOR), Conditional Approval

• Executes operational and compliance activities for assigned deliverables:
  • Generates submission content plans
  • Tracks submission progress and milestones
  • Leverages cross-functional teams and alliance partners as needed

About you

Experience

• BS/BA degree in a scientific discipline or MSc in Biology, Life Science, or related field is required with at least 8 years of relevant pharmaceutical/biotechnology industry experience, including at least 6 years of relevant Regulatory Affairs experience in the oncology therapeutic area OR
• Advanced degree (PharmD, PhD, MD or DVM) with at least 4 years of regulatory or relevant pharmaceutical/biotechnology industry experience required include at least 2 years of relevant Regulatory Affairs experience in the oncology therapeutic area.

Technical Skills

• Understanding of clinical development of drugs and/or innovative biologics products is preferred.
• Demonstrated experience wit