Associate Director, Clinical Pharmacology

Role: Associate Director, Clinical Pharmacology, leading PK/PD-driven clinical pharmacology activities across drug development projects. Responsibilities: independently develop compound strategies, contribute to Phase 2/3 study design and registrational plans, lead Clinical Pharmacology and Pharmacometrics plans, design and analyze studies, and serve as a subject matter expert in regulatory interactions. Collaborate cross-functionally on drug development and provide mentorship within the team. Qualifications: MS, PhD, or PharmD with 5+ years’ experience in Clinical Pharmacology or Pharmacometrics, including expertise with small molecules or biologics in clinical development; strong PK/PD, model-informed drug development, and communication skills; programming experience (e.g., NONMEM, R, WinNonlin) is highly desirable. HighValue: involvement in late-stage clinical development (Phases 2 and 3) across therapeutic areas, utilizing PK/PD modeling, with responsibilities in study design, analysis, and regulatory interactions. WorkSetup: roles are likely hybrid or remote, with no specific travel requirements stated.