Research Investigator, Quantitative Pharmacology

Incyte CorporationWilmington, DE
Onsite

About The Position

A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia. Job Summary (Primary function) The Research Investigator, Pharmacokinetics is responsible for performing PK/PD analysis, population PK/PD analysis, and PBPK for Biologics and small molecules in the clinical pharmacokinetics group.

Requirements

  • Ability to work both independently and collaboratively with diverse teams.
  • Excellent written and verbal communication skills.
  • Experience with a range of software packages, such as but not limited to: WinNonlin, NONMEM, R, SimCyp and GastroPlus.
  • Experience in analyzing clinical pharmacology data.
  • Experience in clinical PK, population PK analysis, and PBPK modeling.
  • Advanced degree (e.g., Ph.D., Master's) in Pharmacokinetics, Pharmacometrics, Pharmacology, Engineering, Statistics, or related fields, or equivalent experience.

Nice To Haves

  • Experience with writing reports for regulatory submissions is desired.
  • Experience in large molecule development is highly preferable.

Responsibilities

  • Present work at internal and external scientific meetings and publish manuscripts in peer-reviewed journals.
  • Work with clinician, biostatistician, and data manager to provide deliverables on time.
  • Represent clinical pharmacokinetics on clinical project teams.
  • Conduct model based simulations using PBPK method to design studies that yield high value PK/PD information for future critical decisions.
  • Perform PK/PD analyses, pop PK/PD analyses, interpret and report data to clinical teams and management in a timely manner.
  • Advise clinical teams on PK and PK/PD study design.
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