Director of Quantitative Pharmacology & Clinical Strategy

Sarepta Therapeutics

New Hampshire

Hybrid

USD 139,000 - 232,000

Full time

14 days+

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Job summary

Sarepta Therapeutics in the United States is seeking a Director of Quantitative & Clinical Pharmacology to lead pharmacology efforts across early to late-stage development, with emphasis on dose selection and PK/PD modeling. The role is highly visible, cross-functional, and requires strategic leadership in modeling and translational science.

The candidate will guide population PK/PD analyses, support regulatory interactions, and stay at the forefront of clinical pharmacology and pharmacometrics.

Qualifications

  • PhD with 7+ years in clinical pharmacology or pharmacometrics.
  • Strong PK/PD modeling and regulatory interaction experience.
  • Excellent communication, multitasking and collaboration skills.
  • Experience in NONMEM & R highly preferred.
  • siRNA and/or CNS experience is preferred.

Responsibilities

  • Lead quantitative pharmacology strategies across all stages of drug development through approval.
  • Provide clinical pharmacology expertise in translational development, protocol prep, study execution, and reporting.
  • Perform model-based analyses (population PK, PK/PD modeling, meta-analysis) to inform development.
  • Serve as functional lead for global regulatory strategies and HA engagements.
  • Maintain cutting-edge knowledge, publish work, and present at scientific venues.

Skills

PK/PD modeling
Nonmem & R
Pharmacomet rics
Communication
Regulatory interactions

Education

PhD in Pharmaceutical Sciences, mathematics/engineering or related field

Tools

NONMEM
R

Job description

Sarepta Therapeutics in the United States is seeking a Director of Quantitative & Clinical Pharmacology to lead pharmacology efforts across early to late-stage development, with emphasis on dose selection and PK/PD modeling. The role is highly visible, cross-functional, and requires strategic leadership in modeling and translational science.

The candidate will guide population PK/PD analyses, support regulatory interactions, and stay at the forefront of clinical pharmacology and pharmacometrics.

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