Global Head, Regulatory Science — Model-enabled Development, Real World Evidence And Novel Endpoints

Sanofi UK

Morristown, NJ, US
Base: $266,250.00 - $384,583.33; bonus/equity: not...
Model-enabled drug development
Real world evidence
Novel endpoints
The Global Head, Regulatory Science — Model-Enabled Development, Real World Evidence & Novel Endpoints serves as a specialized center of excellence within Sanofi's Regulatory framework, driving innovation in regulatory science through advanced model-informed approaches, real world evidence and novel endpoint development

Job Summary

  • The Global Head, Regulatory Science — Model-Enabled Development, Real World Evidence & Novel Endpoints serves as a specialized center of excellence within Sanofi's Regulatory framework, driving innovation in regulatory science through advanced model-informed approaches, real world evidence and novel endpoint development.
  • We accelerate drug development timelines by providing expert guidance on Model-Enabled Drug Development frameworks, regulatory validation of new endpoints, real-world evidence data and cutting-edge regulatory strategies across therapeutic areas.
  • The salary range for this position is: $266,250.00 - $384,583.33 All compensation will be determined commensurate with demonstrated experience.

Matching Summary

The Global Head, Regulatory Science — Model-Enabled Development, Real World Evidence & Novel Endpoints serves as a specialized center of excellence within Sanofi's Regulatory framework, driving innovation in regulatory science through advanced model-informed approaches, real world evidence and novel endpoint development.

Salary

Base: $266,250.00 - $384,583.33; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Model-Enabled Drug Development
  • Real World Evidence
  • Novel Endpoints
  • Regulatory Strategy
  • Health Authority Engagement

Nice-to-have

  • AI-powered research
  • Cross-functional collaboration
  • Patient-focused outcomes
  • Scientific rigor

Key Requirements

  • 10-15 years regulatory affairs experience
  • Direct experience with Model-Informed Drug Development (MIDD)
  • Proven track record of successful regulatory submissions
  • Demonstrated leadership experience
  • Bachelor's degree required
  • Advanced degree highly desirable

Work Rights

Not specified

Tailored Resume

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