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Regulatory Strategist – Sanofi Sanofi

Job in Cherry Hill, Camden County, New Jersey, 08358, USA
Listing for: Biotech Reality
Full Time position
Listed on 2026-07-31
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 148500 - 214500 USD Yearly USD 148500.00 214500.00 YEAR
Job Description & How to Apply Below

Regulatory Strategist jobs at Sanofi are open right now for candidates who want to shape global drug development strategy at one of the world's leading R&D-driven biopharma companies. This particular opening sits within Sanofi's Global Regulatory Team (GRT) and is based in Morristown, New Jersey or Cambridge, Massachusetts, with a disclosed salary range of $148,500-$214,500 USD per year.

Quick Facts
  • Job Title: Regulatory Strategist
  • Company: Sanofi
  • Locations: Morristown, NJ / Cambridge, MA (hybrid/onsite per team)
  • Department: Research and Development
    - Regulatory Affairs
  • Salary Range (Sanofi-disclosed): $148,500-$214,500 / year
  • Apply by: Rolling / Open until filled (confirm on employer site).
  • Role Profile
  • Providing regulatory input to clinical development, commercial, and cross-functional GRT partners.
  • Contributing to the Target Product Profile (TPP), governance, and business planning as part of "one regulatory voice".
  • Developing the Global Regulatory Project Strategy (GRPS) and aligning it with core product labeling.
  • Owning Health Authority engagement plans, including authoring briefing documents and leading HA meetings.
  • Leading submission teams to ensure NDA/BLA/MAA/Extension filings hit launch timelines.
  • Directing IND/CTA submission strategy to keep clinical trial initiation on schedule.
  • Managing submission content planning, tracking, and document management with cross-functional and alliance partners.
  • Also check:
    Senior Biotechnologist
    - Sanofi

    Qualifications and Requirements
  • A BS/BA in a relevant scientific discipline (advanced degree
    - PharmD, PhD, MD, DVM, or MSc - preferred).
  • 6+ years in pharma/biotech, including 4+ years in Regulatory Affairs (regional and global).
  • Experience preparing (s)
    BLA/(s)
    NDA/MAA and IND/CTA filings, plus HA briefing documents.
  • Prior work on multidisciplinary, matrixed project teams.
  • Project leadership experience is a plus.
  • #J-18808-Ljbffr
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