Associate Director, Commercial Regulatory Affairs

Bristol Myers Squibb

Princeton, NJ, United States
Base: $173,350 - $210,058; bonus/equity: + incenti...
50% onsite
Promotional material regulatory advice
Risk assessment and mitigation strategies
Ensure regulatory compliance
The role requires providing regulatory advice, risk assessment, and mitigation strategies to Commercial Teams, Medical Affairs, and other internal groups on promotional materials to ensure company objectives are met

Job Summary

  • The role requires providing regulatory advice, risk assessment, and mitigation strategies to Commercial Teams, Medical Affairs, and other internal groups on promotional materials to ensure company objectives are met.
  • Responsibilities include ensuring full regulatory compliance of all promotions with approved labeling and FDA guidances, leading training on relevant regulations, and monitoring the evolving regulatory landscape.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs to support employees' goals, including health coverage, wellbeing support, financial well-being, and work-life benefits.

Matching Summary

The role requires providing regulatory advice, risk assessment, and mitigation strategies to Commercial Teams, Medical Affairs, and other internal groups on promotional materials to ensure company objectives are met.

Salary

Base: $173,350 - $210,058; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Promotional material regulatory advice
  • Risk assessment and mitigation strategies
  • Ensure regulatory compliance
  • FDA advertising and promotion regulations
  • Develop and maintain strong relationships

Nice-to-have

  • Solution oriented and innovative advice
  • Pursues and understands diverse perspectives
  • Integrate compliance considerations
  • Process improvement and guiding principles

Key Requirements

  • 3-5 years Regulatory promotional review
  • 5-8 years pharmaceutical experience
  • Experience providing risk assessment
  • Ability to propose regulatory strategies
  • Experience communicating and negotiating with OPDP
  • BS required; advanced degree preferred

Work Rights

Not specified

Tailored Resume

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