Director, Infectious Diseases And Vaccines, Quantitative Pharmacology And Pharmacometrics

Merck & Co., Inc.

Base: $190,800.00 - $300,300.00; bonus/equity: ann...
Hybrid
Phd or pharmd with 7-9 years experience
Population pk and pkpd modeling expertise
Regulatory submission document authoring
The Director will apply quantitative approaches to characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and biologics to inform dose selection and regulatory strategies

Job Summary

  • The Director will apply quantitative approaches to characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and biologics to inform dose selection and regulatory strategies.
  • Candidates must demonstrate outstanding leadership skills to mentor junior colleagues and collaborate with cross-functional teams to frame critical drug development questions.
  • This role offers a comprehensive benefits package including medical, dental, vision, 401(k) retirement benefits, and eligibility for annual bonuses and long-term incentives.

Matching Summary

The Director will apply quantitative approaches to characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and biologics to inform dose selection and regulatory strategies.

Salary

Base: $190,800.00 - $300,300.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation

Skills & Requirements

Must-have

  • PhD or PharmD with 7-9 years experience
  • Population PK and PKPD modeling expertise
  • Regulatory submission document authoring
  • NONMEM, R, Matlab, SAS programming skills
  • Infectious disease or vaccine asset experience

Nice-to-have

  • Machine Learning application in pharmacometrics
  • Viral dynamic analysis capabilities
  • Strong interdisciplinary leadership skills
  • Experience with global regulatory meetings
  • Exposure-response and QSP modeling

Key Requirements

  • PhD or PharmD degree required
  • Minimum 7 years (PhD) or 9 years (PharmD) experience
  • Direct experience in regulatory filings for small molecules/biologics
  • Proficiency in NONMEM, Monolix, Phoenix, R, or Matlab
  • US work authorization or VISA sponsorship eligibility

Work Rights

Not specified

Sponsorship: available

Tailored Resume

Cover Letter