Principal Investigator, Clinical Pharmacology & Pharmacometrics
About this opportunity
Overview 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) This position will be responsible for performing pharmacometric modeling and simulations including but not limited to population PK/PD, (semi-)mechanistic PK/PD, PBPK, and QSP, etc., to support early clinical development for biologics and small molecules. Levels will be commensurate with qualifications and experience. Essential Functions of the Job (Key responsibilities) Develop and execute pharmacometric modeling and simulations strategy in support of clinical development programs, regulatory/submission strategy and related documents Perform PK/PD analyses and/or population PK/PD analyses, interpret and report data to clinical teams and management in a timely manner. Perform (semi-)mechanistic PK/PD, PBPK, and/or QSP modeling and simulations that yield high value PK/PD information for critical clinical development decisions. Work with other functions such as clinical development, biostatistics, data management, medical writing, and regulatory affairs, etc., to provide deliverables on time. Present work internally and at external scientific meetings and publish manuscripts in peer-reviewed journals. Qualifications (Minimal acceptable level of education, work experience, and competency) Ph.D. in Pharmacokinetics, Pharmacometrics, Pharmacology, Pharmaceutical Science, Chemical/Biomedical engineering, Statistics or related fields. 1-5 years post-PhD or 3-7 years post-MSc of experience in population PK/PD analysis, PBPK, and/or QSP modeling and simulations. Levels will be commensurate with qualifications and experience. Experience in multiple software packages such as R, NONMEM, Monolix, MatLab, Simcyp, GastroPlus, or other pharmacokinetic, modeling and data visualizations software. Scientific understanding of biopharmaceutical and ADME properties of both small molecules and biologics Experience in scheduling and execution of multiple programs and projects, in a dynamic and cutting-edge research environment; Excellent communication skills (verbal and written) and presentation skills Ability to work independently Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer. We Respect Your Privacy Learn more at: http://www.incyte.com/privacy-policy The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate. During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here. You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work. You can learn more about Incyte’s data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable). Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 295 comparable Principal Clinical Development roles across 54 biopharma companies.
Salary context
120 of 295 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 295 comparable roles
+ 15 more countries
Seniority mix
295 of 295 peers have a known seniority level
Therapeutic area mix
72 of 295 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.