Associate Principal Scientist (associate Director) - Regulatory Liaison

Newyorkbioconnect

North Wales, Pennsylvania, USA
Base: $142,400.00 - $224,100.00; bonus/equity: ann...
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Global regulatory strategy
Regulatory submissions
Agency communications
** The Associate Principal Scientist (Regulatory Liaison) at Newyorkbioconnect is responsible for supporting regulatory strategy and submissions for vaccine and infectious disease products. The role requires strong communication and collaboration skills to work within a global regulatory team and offers a hybrid work model. **

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 registration and maintenance of VID products.
  • Responsibilities include assisting in regulatory agency communications and submissions, implementing strategy for agency background packages, communicating with agencies, and participating as an active member on the Global Regulatory Team.
  • 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 benefits.

Matching Summary

Match Score: 75

** The Associate Principal Scientist (Regulatory Liaison) at Newyorkbioconnect is responsible for supporting regulatory strategy and submissions for vaccine and infectious disease products. The role requires strong communication and collaboration skills to work within a global regulatory team and offers a hybrid work model. **

Salary

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

Skills & Requirements

Must-have

  • Global regulatory strategy
  • Regulatory submissions
  • Agency communications
  • Cross-functional collaboration
  • Research regulatory guidances

Nice-to-have

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