Global Regulatory Lead

Sanofi

Morristown, NJ, US
Base: $178,500.00 - $257,833.33; bonus/equity: not...
Onsite
Global regulatory strategy development
Regulatory submissions and filings
Leadership of regulatory teams
Join Sanofi’s Rare Disease and Rare Blood Disorders Regulatory Team as Global Regulatory Lead responsible for developing and executing global regulatory strategies to meet corporate and business objectives

Job Summary

  • Join Sanofi’s Rare Disease and Rare Blood Disorders Regulatory Team as Global Regulatory Lead responsible for developing and executing global regulatory strategies to meet corporate and business objectives.
  • Sanofi offers a supportive, future-focused environment with opportunities for career growth, a comprehensive rewards package, and extensive health and wellbeing benefits including at least 14 weeks’ gender-neutral parental leave.
  • Sanofi is committed to equal opportunity and affirmative action, fostering a culturally diverse and inclusive workforce that values diverse backgrounds and perspectives.

Matching Summary

Join Sanofi’s Rare Disease and Rare Blood Disorders Regulatory Team as Global Regulatory Lead responsible for developing and executing global regulatory strategies to meet corporate and business objectives.

Salary

Base: $178,500.00 - $257,833.33; Bonus/Equity: Not specified; Benefits: Company employee benefit programs available

Skills & Requirements

Must-have

  • Global regulatory strategy development
  • Regulatory submissions and filings
  • Leadership of regulatory teams
  • Lifecycle management of products
  • Cross-functional team collaboration
  • Regulatory risk assessment and mitigation

Nice-to-have

  • Fostering team performance and coaching
  • Advanced communication and negotiation skills
  • Multicultural and multinational sensitivity
  • Business acumen and leadership presence
  • Creativity and innovation in regulatory strategy
  • Forward-looking team vision and trust building

Key Requirements

  • At least 12 years pharmaceutical/biotech experience
  • Minimum 10 years Regulatory Affairs experience
  • Experience in early and late development
  • Proven leadership in regulatory filings
  • Advanced degree preferred (PharmD, PhD, MD, DVM, MSc)
  • Experience with global regulatory project teams

Work Rights

US and Puerto Rico residents only

Tailored Resume

Cover Letter