Associate Principal Scientist (associate Director) - Regulatory Liaison

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North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: eli...
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Global regulatory strategy implementation
Regulatory agency communications
Regulatory submissions assistance
** The Associate Principal Scientist position at Merck & Co., Inc. focuses on regulatory affairs within the Vaccine and Infectious Disease therapeutic area. The role requires strong communication and collaboration skills to support global regulatory strategies and submissions, necessitating an advanced degree in biological sciences or related fields, alongside relevant industry experience. **

Job Summary

  • The Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team, working closely with global liaisons to develop and implement global strategies for product registration and maintenance.
  • Responsibilities include assisting with regulatory agency communications and submissions, implementing strategy for agency background packages, conducting research on guidances and competitive intelligence, and collaborating with various functional areas.
  • The role offers a salary range of $142,400.00 - $224,100.00, eligibility for annual bonus and long-term incentive, and a comprehensive benefits package including medical, dental, vision, and retirement benefits.

Matching Summary

Match Score: 75

** The Associate Principal Scientist position at Merck & Co., Inc. focuses on regulatory affairs within the Vaccine and Infectious Disease therapeutic area. The role requires strong communication and collaboration skills to support global regulatory strategies and submissions, necessitating an advanced degree in biological sciences or related fields, alongside relevant industry experience. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Global regulatory strategy implementation
  • Regulatory agency communications
  • Regulatory submissions assistance
  • Vaccine and Infectious Disease products
  • Cross-functional team collaboration

Nice-to-have

  • Strong scientific and analytical skills
  • Attention to detail
  • Flexibility required
  • Process improvement initiatives

Key Requirements

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

Work Rights

Not specified

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