Senior Director, Global Regulatory Lead Neuroscience

Bristol Myers Squibb

Princeton, NJ, US
Cambridge crossing: $258,680 - $313,460; princeton...
50% onsite
Global regulatory affairs neuroscience
Neuroscience drug development
Us and international regulatory environment
This role will be a key member of the GRSP Extended Leadership Team to ensure the development, implementation, and alignment of regulatory strategies across projects and the Neuroscience therapeutic area

Job Summary

  • This role will be a key member of the GRSP Extended Leadership Team to ensure the development, implementation, and alignment of regulatory strategies across projects and the Neuroscience therapeutic area.
  • Develop global therapeutic regulatory strategies and operational plans for identified investigational and marketed products, and serve as the primary interface with health authorities on assigned projects.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

This role will be a key member of the GRSP Extended Leadership Team to ensure the development, implementation, and alignment of regulatory strategies across projects and the Neuroscience therapeutic area.

Salary

Cambridge Crossing: $258,680 - $313,460; Princeton - NJ - US: $226,750 - $274,763; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Global Regulatory Affairs Neuroscience
  • Neuroscience drug development
  • US and international regulatory environment
  • Health authority interface
  • Drug research and development process

Nice-to-have

  • Inter-dependent partnering skills
  • Team-oriented
  • Cross-cultural environments
  • Innovative problem solving

Key Requirements

  • MD, PhD or PharmD preferred
  • 8-12 years pharmaceutical industry experience
  • 6-8 years in regulatory affairs
  • Global experience strongly preferred
  • Command of US experience and EU background desired
  • Specific expert in Drug Development/CMC/Pharmtox/Biopharmaceutics/Clinical/Promotional

Work Rights

Not specified

Tailored Resume

Cover Letter