Amgen logo

Principal Scientist - Clinical Pharmacology, Modeling & Simulation

Amgen
Full-time
Remote friendly (South San Francisco, CA)
United States
Clinical Research and Development

Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.

Role Summary

Principal Scientist - Clinical Pharmacology, Modeling & Simulation

Responsibilities

  • Drive innovative modeling and simulation strategies for translational approaches to support clinical dosage selections and clinical study designs.
  • Apply quantitative translational and clinical pharmacology approaches (PK/PD modeling, M-PBPK, M-PBPK-PD, QSP) integrated with emerging ML and Generative AI to guide optimal clinical drug development.
  • Collaborate across therapeutic areas and modalities to inform target patient populations, dosing strategies, and study designs.

Qualifications

  • Basic Qualifications:
    • Doctorate degree and 2 years of Clinical Pharmacology and Modeling & Simulation experience
    • Or Master’s degree and 4 years of Clinical Pharmacology and Modeling & Simulation experience
    • Or Bachelor’s degree and 6 years of Clinical Pharmacology and Modeling & Simulation experience
    • Or Associate’s degree and 10 years of Clinical Pharmacology and Modeling & Simulation experience
    • Or High school diploma / GED and 12 years of Clinical Pharmacology and Modeling & Simulation experience
  • Preferred Qualifications:
    • PhD in Pharmacokinetics or Pharmaceutical Sciences or Pharmacology or Chemical Engineering or equivalent professional degrees (MD, PharmD).
    • 5+ years of experience in Clinical Pharmacology, Modeling & Simulation in the Biotechnology/Pharmaceutical Industry.
    • Hands-on experience with PK/PD, M-PBPK, M-PBPK-PD, and QSP modeling; expert software knowledge.
    • Established track record of Model Based Drug Development (MIDD).
    • Regulatory experience and knowledge of global regulatory requirements; ability to interact with health authorities and author regulatory documents.
    • Experience leading design and implementation of clinical pharmacology and biopharmaceutic studies and integrating results into regulatory filings and product labels.

Skills

  • Quantitative Clinical Pharmacology approaches with focus on PK/PD, M-PBPK, M-PBPK-PD, and QSP modeling
  • Software proficiency for PK/PD, M-PBPK, M-PBPK-PD, and QSP modeling
  • Leadership and collaboration across cross-functional teams

Education

  • Doctorate or Master’s or Bachelor’s or Associate’s or high school with applicable experience as listed in Basic Qualifications
  • PhD preferred for advanced modeling domains

Additional Requirements

  • Willingness to engage with diverse therapeutic areas including oncology, rare diseases, obesity, and cardiovascular disease
  • Ability to work in a fast-paced, collaborative environment and to communicate complex modeling results to non-specialists
Apply now
Share this job