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PK/PD Principal Scientist

Zoetis
Full-time
Remote friendly (United States)
United States
$111,000 - $181,000 USD yearly
Clinical Research and Development

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Role Summary

The Zoetis Veterinary Medicine Research & Development (VMRD) is seeking a talented PK/PD modeler to join our team to discover and develop novel protein therapeutics for veterinary medicine. The successful candidate will be primarily responsible for providing PK/PD modeling and simulation support for projects from early research through late-stage development. This position will require a highly motivated and independent leader who can effectively collaborate with other team members to advance projects.

Responsibilities

  • Independently develop PK, population PK, PK/PD, PBPK, and/or QSP models using in vivo study data from different veterinary species, employing NONMEM, R, Monolix or related software.
  • Collaborate with project teams to use modeling and simulation to help design, optimize or prosecute in vivo PK, PK/PD and clinical studies in line with the strategic direction of the project.
  • Work collaboratively and communicate effectively with multidisciplinary teams to design and prosecute studies in line with the strategic direction of the project.
  • Provide concise technical reports summarizing modeling and simulation work.
  • Present research results to scientific teams, management, and regulatory agencies.
  • Write sections of regulatory submissions and respond to inquiries from regulatory agencies.

Qualifications

  • Ph.D in bioengineering, mathematics, pharmacology or related field with 4 or more years of relevant pharmaceutical development experience
  • Proven ability to apply PBPK, QSP or population PK modeling using NONMEM, R, or related software.
  • Must have excellent verbal & written communication skills
  • Self-starter, able to prioritize work and work efficiently with minimal supervision.

Desirable Skills

  • Strong background in statistics.
  • Experience analyzing PK/PD of biotherapeutics (protein therapeutics).
  • Self-starter, able to prioritize work and work efficiently with minimal supervision.
  • Experience interacting with regulatory agencies.
  • Working knowledge of bioanalytical assays is helpful.
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