Associate Principal Scientist (associate Director) - Regulatory Liaison

Vetamc

North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
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Global regulatory strategy development
Regulatory agency communications
Marketing application submissions
** The Associate Principal Scientist position at Vetamc focuses on regulatory affairs within the Vaccine and Infectious Disease therapeutic area. The ideal candidate will possess strong communication skills and relevant scientific expertise to support global regulatory strategies and submissions. **

Job Summary

  • The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team.
  • Responsibilities may encompass all aspects of planning and implementation of a global regulatory strategy and regulatory submissions including assisting in preparing submissions, protocol review, and conducting research on regulatory guidances or competitive intelligence.
  • The salary range for this role is $142,400.00 - $224,100.00 and the successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

Matching Summary

Match Score: 75

** The Associate Principal Scientist position at Vetamc focuses on regulatory affairs within the Vaccine and Infectious Disease therapeutic area. The ideal candidate will possess strong communication skills and relevant scientific expertise to support global regulatory strategies and submissions. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package including medical, dental, vision, retirement, paid holidays, vacation, and sick days

Skills & Requirements

Must-have

  • Global regulatory strategy development
  • Regulatory agency communications
  • Marketing application submissions
  • Protocol review
  • Regulatory guidances research
  • Cross-functional collaboration

Nice-to-have

  • Excellent communication and collaboration
  • Attention to detail
  • Flexibility
  • Process improvement initiatives

Key Requirements

  • M.D. or Ph.D. or related doctoral degree
  • Master’s degree with at least 3 years of relevant experience
  • Bachelor’s degree with at least 6 years of relevant experience
  • Prior regulatory experience preferred
  • Experience in drug development preferred

Work Rights

Not specified

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