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Executive Director, Clinical Pharmacology/Pharmacometrics

Recursion· Development
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Remote£136.5k - £167.2kFull-timePosted 3w ago

About the role

Lead the clinical pharmacology and pharmacometrics strategy and execution for a portfolio of rare disease and oncology programs within Recursion, coordinating cross-functional teams and regulatory interactions from a remote UK-based position.

Responsibilities

  • Develop the clinical pharmacology and pharmacometric strategies to accelerate and support the overall product development plan. You’ll be the Clinical Pharmacology lead for various programs in clinical development, the representative for regulatory interactions, and propose innovative strategies to get therapies to patients faster.
  • Solve drug development questions/problems by performing and/or overseeing modeling and simulation with various tools to expedite decision making.
  • Design clinical studies. You’ll provide (clinical) pharmacology input on all clinical study designs, from Phase 1-3 and dedicated Phase 1 clinical pharmacology studies.
  • Author review relevant clinical pharmacology sections for regulatory documents, including Investigator's Brochures (IB), INDs, NDAs, and other regulatory submissions. Act as the clinical pharmacology expert during interactions with health authorities.
  • Interface with cross-functional teams. You’ll work closely with clinical study teams, translational teams (DMPK, Translational Modeling and Toxicology), preclinical teams and due diligence teams to ensure clinical pharmacology-related considerations are addressed.

Qualifications

  • Ph.D. in Pharmaceutical Sciences, Pharmacokinetics or related discipline, M.D with a Clinical Pharmacology expertise, or a Pharm D. with a Clinical Pharmacology fellowship, with 10+ years of experience in biotech/pharmaceutical drug development.
  • Demonstrated success leading all clinical pharmacology related aspects of drug development.
  • Ability to work closely with internal and external stakeholders to manage PK, PK-PD, and PK-safety analyses, including non-compartmental analysis, population PK modeling, and PK-PD modeling and simulations to support dose selection, exposure-response and exposure-safety analyses through various phases of drug development.
  • Proficiency with WinNonlin, Monolix, NONMEM, R or other modeling software.
  • Effective skills directed toward driving collaboration, achieving results, influencing, and resolving conflicts across internal and external stakeholders
  • Demonstrated experience responding to regulatory agency questions, preparing clinical pharmacology aspects of regulatory submissions and attending regulatory meetings.
  • Highly motivated, decisive, and results-oriented individual who is proactive, resourceful, and efficient with the flexibility and creativity to excel in and contribute to a rapidly growing drug discovery and development company.
  • "Experience in oncology is preferred, but not required."

Skills

Required:Clinical pharmacology strategyModeling and simulationRegulatory submissions

Benefits

  • annual bonus
  • equity compensation
  • comprehensive benefits package
Last updated Sep 30, 2026. Interested? Apply on the company site.

About Recursion

Pioneering AI Drug Discovery | Recursion

Decoding biology to radically improve lives.

AIdrug discoverybiotechpharmaRecursion OSdatamodelscompute
Company profileWebsite

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