Associate Principal Scientist (associate Director) - Regulatory Liaison

MOBS Lab

North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: eli...
Hybrid - 3 days in office per week
Global regulatory strategy development
Regulatory agency communications
Regulatory submissions
MOBS Lab is seeking an Associate Principal Scientist to join their Global Regulatory Affairs and Clinical Safety team focused on Vaccine and Infectious Disease. The ideal candidate will possess strong communication and organizational skills, with a background in regulatory affairs, drug development, and relevant scientific qualifications

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.
  • Responsibilities include assisting in regulatory agency communications and submissions, implementing strategy for agency background packages, and conducting research on regulatory guidances.
  • The role offers a hybrid work model with a salary range of $142,400.00 - $224,100.00, eligibility for annual bonus and long-term incentive, and a comprehensive benefits package.

Matching Summary

Match Score: 85

MOBS Lab is seeking an Associate Principal Scientist to join their Global Regulatory Affairs and Clinical Safety team focused on Vaccine and Infectious Disease. The ideal candidate will possess strong communication and organizational skills, with a background in regulatory affairs, drug development, and relevant scientific qualifications.

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, retirement, paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Global regulatory strategy development
  • Regulatory agency communications
  • Regulatory submissions
  • Cross-functional team collaboration
  • Scientific and analytical skills

Nice-to-have

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

Key Requirements

  • MD or PhD 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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