Sumitovant is the parent company of five biopharmaceutical companies: Myovant, Urovant, Enzyvant, Altavant and Spirovant. Our companies have a robust pipeline of innovative drug treatments targeting a broad range of diseases. With a technology-enabled approach to drug discovery, development and commercialization, we remove friction from the process of bringing promising new compounds to market.

The Head of Clinical Pharmacology will provide clinical pharmacology technical expertise and clinical pharmacology strategy on the Advanced Comprehensive Execution and Strategy (ACES) team.  You will be responsible for technical diligence activities, clinical development planning, and execution of clinical pharmacology activities as required (phase 1 studies, exploratory pharmacometric analyses) via internal or external resource.  You will also be responsible for transitioning clinical pharmacology activities/plans to existing vants or implementing appropriate resourcing strategies for new pharma vants.

At Sumitovant You Will:

  • Serve as the clinical pharmacology lead for technical diligence activities
  • Develop clinical pharmacology strategy for assets or assets of interest
  • Design, interpret, and/or conduct clinical pharmacology studies or analyses and provide clinical pharmacology support to Sumitovant, vants and DSP
  • Select Phase 1 units as needed to execute clinical program
  • Oversee and implement clinical pharmacology business initiatives and applications
  • May manage direct reports and/or supervise vendors
  • Serve as the Development Asset Development Lead for selected assets
  • Where needed, prepare and present at Sumitovant or DSP governance meetings
  • May be embedded in a Vant to provide Clinical Pharmacology expertise and support
  • Manage and coach staff, maintain a clinical pharmacology community of practice across pharma vants
  • Provide Clinical pharmacology support to Roivant Sciences, Inc. under service agreement, as necessary

Who You Are:

  • MD, PharmD, or PhD degree
  • Minimum 10 years of experience in the pharmaceutical industry that include conducting and managing pharmacokinetic and pharmacodynamic analyses
  • Experience includes a clinical pharmacology leadership role on a drug development project team
  • Proven track record of clinical pharmacology/pharmacometrics support for regulatory interactions
  • Experience and expertise in Population PK/PD Modeling and/or PBPK modeling

 

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