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Director, Clinical Pharmacology

Madrigal Pharmaceuticals
Full-time
Remote friendly (Conshohocken, PA)
United States
$221,000 - $271,000 USD yearly
Clinical Research and Development

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Role Summary

Director, Clinical Pharmacology. We are seeking a highly skilled Clinical Pharmacologist to join our R&D team to lead Clinical Pharmacology strategy, develop and implement model-informed drug development (MIDD) plans, and contribute to regulatory submissions for programs from IND through NDA/BLA/MAA and post-approval activities.

Responsibilities

  • Responsible for Clinical Pharmacology strategy within projects
  • Represent Clinical Pharmacology and contribute to integrated strategy on development teams, governance meetings, and regulatory engagement with health authorities
  • Serve as a Clinical Pharmacology subject matter expert; develop, review, and approve Clinical Pharmacology content across company documents
  • Support strategy for dose selection, dose justification, and regulatory filings
  • Assess and inform bioanalytical planning and methods
  • Lead design of Clinical Pharmacology studies and associated data analysis, interpretation, and reporting
  • Provide input to Phase 1-4 clinical study design and registrational strategy
  • Develop and execute model-informed drug development (MIDD) strategy, including vendor management
  • Provide expertise to Business Development to assess external opportunities

Qualifications

  • Advanced Degree in pharmacology, pharmaceutical sciences, chemical/biomedical engineering or related field (Ph.D. or PharmD)
  • 12-15 years of experience at Director level, with relevant industry background
  • Experience characterizing PK/PD properties of small molecules and biologics
  • Experience applying Clinical Pharmacology in early and late-stage drug development
  • Experience preparing regulatory submissions (IND, CTA, PIP/PSP, NDA, BLA, MAA) and responding to health authorities
  • Prior experience in MASH/metabolic diseases is a plus but not required

Skills

  • Ability to work in a dynamic, team-oriented environment
  • Stakeholder management with strong influence/leadership
  • Quantitative data analysis and data visualization skills
  • Proficiency with data analysis and modeling tools (e.g., NONMEM, Phoenix WinNonlin, R, MATLAB, Monolix, SAS)
  • Proficiency in MIDD principles and analyses (PopPK/PD, E-R, PBPK, QSP, MBMA)
  • Knowledge of bioanalytical methods and associated guidances is a plus
  • Team-oriented mindset and ability to establish high-quality Clinical Pharmacology deliverables

Education

  • Advanced degree (Ph.D. or PharmD) in pharmacology, pharmaceutical sciences, or related field
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