Associate Principal Scientist (associate Director) - Regulatory Liaison

Merck & Co., Inc.

North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
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Global regulatory strategy implementation
Regulatory agency communications
Regulatory submission preparation
** Merck & Co., Inc. is seeking an Associate Principal Scientist in Regulatory Affairs for its Vaccine and Infectious Disease therapeutic area. The role requires strong communication skills and a background in regulatory strategy, focusing on product registration and maintenance. This hybrid position allows for three days in-office work per week. **

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

** Merck & Co., Inc. is seeking an Associate Principal Scientist in Regulatory Affairs for its Vaccine and Infectious Disease therapeutic area. The role requires strong communication skills and a background in regulatory strategy, focusing on product registration and maintenance. This hybrid position allows for three days in-office work per week. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Global regulatory strategy implementation
  • Regulatory agency communications
  • Regulatory submission preparation
  • Cross-functional team collaboration
  • Research regulatory guidances

Nice-to-have

  • Excellent communication and collaboration skills
  • Flexibility and adaptability
  • Attention to detail
  • 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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