Manager, Clinical Pharmacology


Princeton
Permanent
$130,000 - $150,000 USD a year
Research and Development
PR/604132_1786712880
Manager, Clinical Pharmacology

Title: Manager / Senior Manager, Clinical Pharmacology

Location: Princeton, New Jersey (Hybrid)

This pharmaceutical company is seeking an experienced Clinical Pharmacologist to provide strategic and scientific leadership across multiple drug development programs. A successful candidate will leverage pharmacokinetic (PK), pharmacodynamic (PD), and quantitative clinical pharmacology principles to inform key development decisions, including dose optimization, study design, and benefit-risk assessments.

Key Responsibilities:

  • Serve as the clinical pharmacology lead for one or more development programs across various stages of clinical development.
  • Develop and implement clinical pharmacology strategies that support program objectives and regulatory requirements.
  • Provide scientific input into clinical study protocols, statistical analysis plans, clinical study reports, investigator brochures, and regulatory documents.
  • Lead the interpretation and integration of PK, PD, exposure-response, and translational data to support development decisions.
  • Evaluate dose selection strategies and recommend dosing regimens based on available preclinical and clinical data.
  • Author, review, and contribute to clinical pharmacology sections of regulatory submissions and responses to health authorities.
  • Manage and oversee external vendors, consultants, and contract research organizations supporting clinical pharmacology activities.

Qualifications:

  • PhD, PharmD, MD, or equivalent advanced degree in Clinical Pharmacology, Pharmacology, Pharmaceutical Sciences, or a related scientific discipline.
  • Minimum of 5 years of industry experience in clinical pharmacology or a closely related function within biotechnology, pharmaceutical, or life sciences organizations.
  • Demonstrated experience leading clinical pharmacology activities for development programs across multiple clinical phases.
  • Strong understanding of pharmacokinetics, pharmacodynamics, dose-exposure-response relationships, and model-informed drug development principles.

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