Senior Clinical Pharmacologist (Oncology)

Role: Lead Clinical Pharmacology Scientist supporting Phase 1-4 clinical studies, focusing on PK/PD modeling, proposal development, and methodological innovation. Responsibilities: design and optimize clinical pharmacology strategies, author regulatory and scientific documents (protocols, reports, filings), conduct data analyses including modeling, and present findings internally and at conferences. Collaborate across clinical, CMC, and regulatory teams to provide integrated pharmacology input. Requirements: PhD in a relevant field (PK, PBPK, Pharmacometrics) with typically 0+ years (PhD) to 8+ years (Master's) of experience; strong scientific acumen, interpersonal skills, and ability to work in cross-functional teams. Preferred skills include expertise in PK/PD modeling, regulatory writing, and clinical pharmacology strategies. High-Value: involvement in early to late-phase clinical development, expertise in PK/PD, modeling/simulation, and contributions to regulatory submissions. Work Setup: not specified.