Associate Director, Clinical Pharmacology (Immunology)

Role: Lead Clinical Pharmacology strategy for biopharma development programs, spanning Phase 1-4 studies, with a focus on PK/PD modeling and regulatory support. Responsibilities: design and execute clinical pharmacology plans, author regulatory documents, lead cross-functional meetings, provide scientific input at regulatory interactions, and represent pharmacology in business development. Qualifications: PhD with 4+ years or PharmD with 6+ years in PK, PBPK, PK/PD, Pharmacometrics, or systems pharmacology; proven scientific and leadership skills; experience with biologics or small molecules in clinical development. HighValue: expertise in clinical pharmacology, regulatory documentation, cross-functional collaboration, and leadership within biopharma, supporting projects from early to late-stage development. WorkSetup: not specified; likely hybrid or onsite based on typical roles.