Director, Pharmacometrics

SwitzerlandCompetitiveRemote0 applicants

About this role

Step into a role where science meets strategy and your expertise shapes the future of drug development. As a Director, Pharmacometrician, you’ll lead high-impact modeling and simulation efforts within a dynamic Clinical Pharmacology, Modeling and Simulation (CPMS) environment. You’ll guide teams, mentor pharmacometricians, and provide strategic insight to clients at key development milestones. This role also offers the opportunity to represent clients in interactions with regulatory agencies. If you thrive on collaboration and solving complex scientific challenges, this is your chance to make a meaningful impact.

About the role

This role combines scientific leadership and strategic impact, leading population PK analyses while developing innovative approaches to improve efficiency and accuracy. You will design, analyze, and interpret clinical pharmacology studies, provide strategic guidance to clients, and contribute to regulatory documents and agency interactions. In addition, you’ll foster client relationships, support business development, and stay at the forefront of PK/PD advancements to drive continuous improvement.

Your main responsibilities will include but not limited to:

Lead and conduct population PK analyses using advanced modeling tools and methodologies

Develop and implement innovative approaches to enhance the efficiency and accuracy of PK analysis

Design, analyze, and interpret clinical pharmacology studies (renal, hepatic, TQT, ADME, DDI, BE/BA, SAD, MAD, etc.) and provide guidance to optimize pharmacokinetic sampling and dosing strategies

Provide strategic guidance to clients, owning deliverables and developing clinical pharmacology plans

Author and review PK reports and clinical pharmacology sections of regulatory documents

Represent clients in regulatory interactions and contribute to business development and relationship management

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Responsibilities

  • Lead and conduct population PK analyses using advanced modeling tools and methodologies
  • Develop and implement innovative approaches to enhance the efficiency and accuracy of PK analysis
  • Design, analyze, and interpret clinical pharmacology studies (renal, hepatic, TQT, ADME, DDI, BE/BA, SAD, MAD, etc.) and provide guidance to optimize pharmacokinetic sampling and dosing strategies

Requirements

  • Provide strategic guidance to clients, owning deliverables and developing clinical pharmacology plans
  • Author and review PK reports and clinical pharmacology sections of regulatory documents
  • Represent clients in regulatory interactions and contribute to business development and relationship management

EU Requirements

Job Details

Posted28 September 2026
Closes28 October 2026
Work ModeRemote

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