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Director, Pharmacokinetics

Job in West Point, Montgomery County, Pennsylvania, 19486, USA
Listing for: MSD
Full Time position
Listed on 2026-10-13
Job specializations:
  • Research/Development
    Pharmaceutical Science/ Research, Drug Discovery, Research Scientist
Salary/Wage Range or Industry Benchmark: 173200 - 272600 USD Yearly USD 173200.00 272600.00 YEAR
Job Description & How to Apply Below
Location: West Point

The Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) function of our Research & Development Division, is seeking a dynamic and collaborative individual to lead a team of scientists in the Drug Metabolism and Pharmacokinetics (DMPK) group in West Point, Pennsylvania. The team primarily supports discovery programs across modalities (small molecules and conjugates) and therapeutic areas, enabling strategic decisions from lead selection through FIH.

As Director in the West Point DMPK group, your main responsibility is leading a motivated team of experienced Scientists representing the department in cross‑functional teams as well as a group of bench scientists, charged with conducting mechanistic ADME studies. The position requires a focus on talent development as well as scientific creativity. The DMPK director must be able to work collaboratively in a fast‑paced environment, drive innovation, and have excellent scientific, interpersonal and communication skills in order to guide the team on the design, implementation and interpretation of in silico, in vitro and in vivo studies necessary to influence decisions in drug discovery and development.

The ideal candidate will have an in‑depth understanding of ADME, as well as pharmacokinetic and PK/PD principles that impact the discovery and development of new chemical entities. Experience with small molecules drug discovery is expected and additional experience with various drug modalities across therapeutic areas is desired. The candidate should be familiar with PK, PK/PD and PBPK modeling as tools to drive decision making.

We are highly engaged in influencing the success of a large and exciting portfolio and continue to evolve the influence of new computational and laboratory techniques towards the selection of differentiated products. This role provides a unique opportunity to influence our evolving pipeline while enabling the growth of the next generation of leaders.

Education Minimum Requirement:
  • PhD. in chemistry, Pharmaceutical Sciences, Pharmacology, Biomedical Engineering, Biochemistry, or related field with 8+ years of experience supporting drug discovery in the Pharmaceutical Industry.
  • Applicants with MSci. degree with 12+ years relevant industry experience will be considered.
Required

Experience and Skills:
  • Experienced in providing DMPK support in drug discovery programs, including assessment of tractability, dose and PK predictions, drug metabolism, assessment of drug interaction risk and communicating analyses and recommendations to interdisciplinary teams and management.
  • Experienced in integrating preclinical ADME, PK, and pharmacology data to enable translational PK/PD modeling and simulation to support dose selection, design of PK/PD and safety assessment studies, and dose justifications for preclinical and clinical studies.
  • Knowledge of cutting-edge in silico approaches to inform decision making related to the characterization of metabolism, drug interactions, exposure-response relationships and variability.
  • Knowledge of modern instrumentation in support of DMPK workflows.
  • Strong leadership, interpersonal, communication, problem solving, and collaboration skills along with strength in delivering results on firm deadlines.
  • At least 3 years’ experience with management or supervision of staff.
  • A strong aptitude for and previous experience in managing scientific teams and attracting, developing, and retaining talent.
  • Excellent verbal and written communications skills and an ability to excel in a team-based environment.
Preferred

Experience and Skills:
  • Experience with authoring documents in support of regulatory filings, including IBs, INDs and CTDs as well as responses to regulatory questions.
  • Experience with evaluation of…
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