Director of Clinical Pharmacology Job at EPM Scientific, Trenton, NJ

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  • EPM Scientific
  • Trenton, NJ

Job Description

EPM Scientific is currently partnered with a biopharmaceutical company is dedicated to the discovery, development, and commercialization of treatments for multiple assets and programs. With a strong foundation in neuroscience and a commitment to addressing unmet medical needs, the organization leverages cutting-edge science and a patient-focused approach to bring transformative therapies to market. Its pipeline includes both early- and late-stage assets, reflecting a strategic focus on delivering impactful solutions across a range of neurological and psychiatric conditions.

The Director of Clinical Pharmacology & Pharmacometrics will lead the strategic and operational aspects of clinical pharmacology and pharmacometric activities across the drug development lifecycle. This individual will play a critical role in optimizing dose selection, trial design, and regulatory strategy through the application of quantitative pharmacology and model-informed drug development (MIDD) principles.

Key Responsibilities:

  • Lead the design, execution, and interpretation of clinical pharmacology studies (e.g., ADME, PK/PD, drug-drug interaction, special populations).
  • Develop and implement pharmacometric strategies including population PK, exposure-response, and disease progression modeling.
  • Collaborate cross-functionally with clinical development, regulatory affairs, biostatistics, and nonclinical teams to support program goals.
  • Represent clinical pharmacology in regulatory interactions and contribute to the preparation of regulatory submissions (e.g., INDs, NDAs, briefing documents).
  • Provide scientific leadership in the application of MIDD to inform decision-making and accelerate development timelines.
  • Oversee external vendors and consultants involved in pharmacokinetic and pharmacometric analyses.
  • Mentor and develop junior staff within the clinical pharmacology and pharmacometrics function.

Qualifications:

  • PhD, PharmD, or MD in Clinical Pharmacology, Pharmaceutical Sciences, or a related discipline.
  • Minimum of 10 years of experience in the pharmaceutical or biotechnology industry, with a strong background in clinical pharmacology and pharmacometrics.
  • Proven track record of successful regulatory submissions and interactions.
  • Expertise in modeling and simulation tools (e.g., NONMEM, Monolix, Phoenix WinNonlin, R).
  • Strong understanding of regulatory guidance and global expectations for clinical pharmacology.
  • Excellent communication, leadership, and project management skills.

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