Associate Principal Scientist (associate Director) - Regulatory Liaison

Merck Sharp & Dohme Corp

North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
Hybrid (3 days in office, 1 day remote)
Global regulatory strategy
Regulatory agency communications
Regulatory submissions
Merck Sharp & Dohme Corp is seeking an Associate Principal Scientist to support the regulatory affairs team in the Vaccine and Infectious Disease therapeutic area. The ideal candidate will have strong communication skills and relevant experience in regulatory submissions, with a focus on vaccine and anti-infective products

Job Summary

  • The Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team, developing and implementing global strategies for registration and maintenance.
  • Responsibilities include assisting in regulatory agency communications and submissions, implementing strategy for marketing applications, and conducting research on regulatory guidances.
  • The role involves collaboration with various functional areas and supports the maintenance of VID programs, including label development and process improvement initiatives.

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking an Associate Principal Scientist to support the regulatory affairs team in the Vaccine and Infectious Disease therapeutic area. The ideal candidate will have strong communication skills and relevant experience in regulatory submissions, with a focus on vaccine and anti-infective products.

Salary

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

Skills & Requirements

Must-have

  • Global regulatory strategy
  • Regulatory agency communications
  • Regulatory submissions
  • Cross-functional teamwork
  • Scientific and analytical skills

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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