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

Role: Senior/Associate Director in Clinical Pharmacology leading PK/PD strategies across multiple development phases (Phases 1-4) with a focus on biologics or small molecules. Responsibilities: design and oversee clinical pharmacology studies, author regulatory documents, lead cross-functional teams, drive study analyses and interpretation, represent pharmacology in strategic and regulatory meetings, and contribute to scientific publications and presentations. Qualifications: PhD with 4+ years or PharmD with 6+ years in pharmacometrics, PK, PBPK, or related fields; proven leadership, strategic thinking, and excellent interpersonal skills. Senior level typically requires 8+ years of relevant experience; associate level 4+ years. High-value: experience in clinical pharmacology in biopharma, with emphasis on immunology, oncology, or neuroscience; development stage includes Phases 1-4; regulatory engagement and scientific dissemination are key. Collaboration involves internal cross-functional teams, external KOLs, and regulatory agencies. Work setup details not specified.