• Facilitate generation of, author, update, and/or review key documents, including, but not limited to: Protocol concepts, synopses, protocols, and amendments; Informed consent documents; Investigator Brochures; Clinical study reports; Abstracts, posters and manuscripts; Clinical sections of INDs (and equivalent applications), NDAs (and equivalent applications), Annual Reports, and Developmental Safety Update Reports; Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports; Risks / benefits analysis for applicable documents; Clinical Development Plans. • Partner with clinical operations and other functional areas for the successful implementation and execution of clinical studies. • Provide scientific expertise for selection of investigator and vendors. • Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol. • Provide scientific and medical support throughout conduct of a clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO’s. • Review, query, and analyze clinical trial data. • Interpret, and present clinical trial data both internally and externally. • Represent a clinical study or development program on one or more teams or subteams. • Create clinical study or program-related slide decks for internal and external use. • Build and maintain opinion leader/investigator networks; organize and present at key opinion leader advisory boards and investigator meetings. • Contribute to or perform therapeutic area/indication research and competitor analysis. • Build strong relationships with internal experts. • Identify continuous process improvement opportunities. • Identify incremental organizational resource needs – staff, budget, and systems. • Develop, track, execute and report on goals and objectives. • Support budget planning and management. • Be accountable for compliant business practices.