• Support BeOne Clinical and Medical assets by successful execution of clinical development programs • Develop clinical program strategy and assure that activities are executed within expected scope, budget and timelines • Work closely with colleagues in clinical development, program leadership, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics, and translational research • Facilitate generation, author, update, and/or review key documents including Protocol concepts, protocols, informed consent documents, clinical study reports, etc. • Partner with clinical operations for the successful implementation and execution of clinical studies • Provide scientific expertise for selection of investigator and vendors • Review, query, and analyze clinical trial data • Create clinical study or program-related slide decks for internal and external use