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Senior Clinical Pharmacologist - Oncology Biotech

Job in Princeton, Mercer County, New Jersey, 08543, USA
Listing for: SystImmune
Full Time position
Listed on 2026-07-23
Job specializations:
  • Research/Development
    Clinical Research, Research Scientist, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 90000 - 140000 USD Yearly USD 90000.00 140000.00 YEAR
Job Description & How to Apply Below

Syst Immune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi‑specific, multi‑specific antibodies, and antibody‑drug conjugates (ADCs). Syst Immune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, Syst Immune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND‑enabling stages, representing cutting‑edge biologics development.

The Scientist/Sr. Scientist, Clinical Pharmacology will support the design, execution, and analysis of clinical pharmacology studies to support drug development programs. This role will contribute to pharmacokinetics (PK), pharmacodynamics (PD), and regulatory strategy to optimize study design, data interpretation, and regulatory submissions. The successful candidate will be expected to both conduct hands‑on PK/PD modeling and simulation and provide strategic leadership across programs.

This role will collaborate cross‑functionally to advance Syst Immune’s pipeline of innovative oncology therapeutics and represent clinical pharmacology in regulatory interactions. It will be able to function in a blended role that includes both classical clinical pharmacology skillsets combined with quantitative analysis skills.

This is a full-time onsite position at our Princeton, NJ location.

Responsibilities
  • Contributes to clinical development strategies of pipeline products across various therapeutic areas and design of clinical studies with some supervision.
  • Collaborate closely with preclinical, clinical, regulatory, biostatistics, and medical affairs teams to drive drug development programs and contribute to trial designs, dosing strategies, and regulatory submissions and interactions with health authorities.
  • Lead the design, validation, and implementation of pharmacometric models to inform decision‑making at various stages of drug development.
Pharmacometrics development, PK and PK/PD analysis, and documentation
  • Conduct modeling and simulation work on PopPK, ER, PK/PD or exploratory analyses and guide PK/PD modeling or simulations as appropriate to inform study design, dose selection, optimization, and efficacy/safety assessments.
  • Contributes to and owns modeling and simulation plan and prepares submission packages.
  • Utilize modeling software such as NONMEM®, R, or other relevant tools to perform data analysis and generate modeling results.
  • Manages data analysis, interpretation, and reporting with some supervision.
  • Evaluates and applies new data and data analyses to refine studies in the development plan.
  • Stays current with the latest advancements in pharmacometric methodologies, applying innovative techniques to enhance modeling practices.
  • Integrates all available data (both clinical and non‑clinical data) into the clinical development strategy from a CP point of view.
  • Mentors and guides junior pharmacometricians, fostering a culture of continuous learning and development within the team.
  • Responsible for clinical pharmacology data package for NDA and responding to regulatory authority queries in the assigned project(s).
  • Carries out functional responsibilities in accordance with applicable SOPs and regulatory requirements.
Qualifications
  • Ph.D., Pharm.

    D., or equivalent with minimum 2 years of relevant experience; or MS or equivalent with minimum 4 years of relevant experience; or equivalent level of expertise and experience.
  • Postdoctoral experience, hospital experience, and industry experience are preferred.
  • Proficient in developing NCA analysis, PopPK, PK/PD, ER analysis, model‑informed drug development (MIDD) principles, and data visualization, results interpretation, and reporting.
  • Proficiency in modeling software such as NONMEM, R, Win Nonlin, Phoenix, etc.
  • Good knowledge and experience of drug development in one or multiple therapeutic areas. Critical thinking skills, with keen scientific and development judgment.
  • Self‑motivated performance and ability to work on teams and in a matrix…
Position Requirements
10+ Years work experience
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