Associate Principal Scientist (associate Director) - Regulatory Liaison

539

North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
**
Global regulatory strategy implementation
Regulatory agency communications
Regulatory submission preparation
** The Associate Principal Scientist position in Global Regulatory Affairs focuses on supporting regulatory strategies for Vaccine and Infectious Disease products. The role requires strong communication and collaboration skills, as well as relevant experience in regulatory submissions and drug development. **

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; The successful candidate will be eligible for annual bonus and long-term incentive, if applicable; We offer a comprehensive package of benefits.

Matching Summary

Match Score: 75

** The Associate Principal Scientist position in Global Regulatory Affairs focuses on supporting regulatory strategies for Vaccine and Infectious Disease products. The role requires strong communication and collaboration skills, as well as relevant experience in regulatory submissions and drug development. **

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Comprehensive package including medical, dental, vision, retirement, paid holidays, vacation, compassionate and sick days

Skills & Requirements

Must-have

  • Global regulatory strategy implementation
  • Regulatory agency communications
  • Regulatory submission preparation
  • Cross-functional team collaboration
  • 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
  • Experience in drug development

Work Rights

Not specified

Tailored Resume

Cover Letter