Senior Clinical Pharmacology & Quantitative Modeling Lead

Moderna Therapeutics Inc.

United States

Remote

USD 100,000 - 147,000

Full time

2 days ago
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Benefits offered by this job

Healthcare benefits
Well-being resources
Paid time off
Global recharge days

Job summary

Moderna Therapeutics Inc. is seeking a highly qualified Clinical Pharmacology expert to drive quantitative strategies across oncology, immunology, and rare disease programs.

You will integrate nonclinical and clinical data to inform dose selection, design, and regulatory interactions, partnering with Pharmacometrics and QSP teams. You will apply PK/PD modeling, translational sciences, and diverse software tools to influence first-in-human decisions, IND submissions, and lifecycle management of

Qualifications

  • PhD in Clinical Pharmacology, Pharmacometrics, Pharmaceutics, statistics or related field.
  • Strong knowledge of quantitative pharmacology methods and translational sciences.
  • Experience supporting first-in-human predictions and regulatory decisions.
  • Experience with oncology, immune therapeutics or rare diseases is a plus.

Responsibilities

  • Develop quantitative strategies and dose selection for programs.
  • Perform PK/PD analyses and interpret model outputs for decision making.
  • Integrate nonclinical and clinical data to support development plans.
  • Collaborate with cross-functional teams on modeling needs and IND submissions.
  • Contribute to regulatory documentation and scientific communications.

Skills

PK/PD modeling
Exposure‑response analysis
Modeling & simulation
Translational PK/PD
Data analysis & visualization
Regulatory strategy knowledge

Education

PhD in Clinical Pharmacology or related field

Tools

R
Phoenix WinNonlin
NONMEM
Monolix

Job description

Moderna Therapeutics Inc. is seeking a highly qualified Clinical Pharmacology expert to drive quantitative strategies across oncology, immunology, and rare disease programs.

You will integrate nonclinical and clinical data to inform dose selection, design, and regulatory interactions, partnering with Pharmacometrics and QSP teams. You will apply PK/PD modeling, translational sciences, and diverse software tools to influence first-in-human decisions, IND submissions, and lifecycle management of

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