Associate Director, Clinical Pharmacology/ Senior Clinical Pharmacologist (Oncology)

Role: Senior Clinical Pharmacologist responsible for leading and executing clinical pharmacology strategies across multiple development phases (Phases 1-4). Objectives include designing and overseeing PK/PD studies, developing new study proposals, and ensuring compliance with regulatory requirements to support drug development and commercialization. Responsibilities encompass leading clinical pharmacology and biopharmaceutics teams, authoring regulatory documents, participating in cross-functional teams, conducting data analysis and interpretation, and representing Clinical Pharmacology in regulatory and business development settings. Requirements: PhD with 4+ years (or PharmD with 6+ years, or extensive experience as detailed), expertise in PK, PBPK, PK-PD, pharmacometrics, or systems pharmacology; strong scientific and technical acumen; excellent interpersonal and leadership skills. Preferred qualifications include demonstrated strategic thinking, influence, and record of scientific contributions. High-value details: Focus on biologics/therapeutic areas include immunology, oncology, neuroscience; involved in early to late-stage development; regulatory interaction and clinical trial design; cross-functional collaboration with clinical, CMC, and regulatory teams. Work environment: not specified in description.