Associate Director, Quantitative Clinical Pharmacology

Sarepta Therapeutics Inc

United States
Base: $160,800 - $201,000; bonus/equity: not speci...
Hybrid
Quantitative modeling methodologies
Population pk, pkpd, disease progression modeling
Integrate, analyze, interpret diverse data
The Associate Director, Quantitative Clinical Pharmacology is responsible for providing translational, clinical pharmacology, and pharmacometrics deliverables for development assets from pre-IND to Phase III

Job Summary

  • The Associate Director, Quantitative Clinical Pharmacology is responsible for providing translational, clinical pharmacology, and pharmacometrics deliverables for development assets from pre-IND to Phase III.
  • The role drives the development and execution of quantitative pharmacology strategies across all stages of development through product registration and leads clinical pharmacology expertise in clinical and translational development strategies.
  • Sarepta Therapeutics offers a competitive compensation and benefit package, including support for Physical and Emotional Wellness, Financial Wellness, and Caregivers.

Matching Summary

The Associate Director, Quantitative Clinical Pharmacology is responsible for providing translational, clinical pharmacology, and pharmacometrics deliverables for development assets from pre-IND to Phase III.

Salary

Base: $160,800 - $201,000; Bonus/Equity: Not specified; Benefits: Competitive package

Skills & Requirements

Must-have

  • Quantitative modeling methodologies
  • Population PK, PKPD, disease progression modeling
  • Integrate, analyze, interpret diverse data
  • Dose selection and key predictors
  • Clinical pharmacology strategies
  • Regulatory strategies and documents

Nice-to-have

  • Solution-oriented, critical thinkers
  • Comfortable with ambiguity and candor
  • Kindness and integrity
  • Leading-edge knowledge
  • Publish manuscripts, present at conferences

Key Requirements

  • PhD in Pharmaceutical Sciences, mathematics/engineering or related field
  • Minimum 5 years experience
  • Hands-on PK/PD modeling analysis
  • Experience in regulatory interactions
  • Experience developing advanced models
  • Skilled in NONMEM, R, Phoenix
  • Authorized to work in the U.S.

Work Rights

Authorized to work in the U.S.

Tailored Resume

Cover Letter