Associate Principal Scientist (associate Director) - Regulatory Liaison

Mericalherbs

North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: eli...
Hybrid (3 days in-office, remote on fridays)
Global regulatory strategy implementation
Regulatory agency communications
Regulatory submissions preparation
Mericalherbs is seeking an Associate Principal Scientist (Associate Director) for their Global Regulatory Affairs and Clinical Safety team, focusing on Vaccine and Infectious Diseases. The ideal candidate will possess strong regulatory knowledge and communication skills to support product registration and maintenance efforts

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 in regulatory agency communications and submissions, implementing strategy for agency background packages, conducting research on regulatory guidances, 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 plans.

Matching Summary

Match Score: 85

Mericalherbs is seeking an Associate Principal Scientist (Associate Director) for their Global Regulatory Affairs and Clinical Safety team, focusing on Vaccine and Infectious Diseases. The ideal candidate will possess strong regulatory knowledge and communication skills to support product registration and maintenance efforts.

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 preparation
  • Cross-functional team collaboration
  • Research regulatory guidances

Nice-to-have

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

Key Requirements

  • MD or PhD or related doctoral degree
  • Master's degree with 3 years experience
  • Bachelor's degree with 6 years experience
  • Prior regulatory experience preferred
  • Experience in drug development preferred

Work Rights

Not specified

Tailored Resume

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