Senior Medical Director, Product Safety Physician Lead

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. The Senior Medical Director serves as the Lead Product Safety Physician for multiple or large complex strategically important developmental programs (often multi-indication) and creates and maintains a single interpretation of global safety data for developmental. With the support of Safety Physicians and Safety Scientists identifies and manages the documentation and communication of safety concerns and together with teams engaged in BeOne sponsored studies, ensures the safety of patients. Essential Functions of the Job: - Accountable for oversight of benefit/risk safety profile of allocated products through the product life cycle with a principle focus on early development - Actively leads and enhances knowledge of safety profiles for allocated products, including both BeOne and competitor products - Identifies and actively leads management of safety concerns for developmental and approved BeOne products - Actively leads Development and, as required, Medical Affairs product teams in the identification of, and handling of product safety concerns - Governance: - Chairs Safety Management Team (SMT) meetings for assigned products, reviews SMT materials, develops & represents safety perspective in SMT meetings - Represents the SMT and participates in Company Safety Committee (CSC) meetings, support meeting preparations, develop & proposes review topics/ CSC agenda items - Actively leads communication of recommendations to labeling group/other stakeholders - Actively participates in meetings as required in External Safety Monitoring Committees (DMC) meetings through provision and review of safety data, insights and leadership and provides input to DMC Charters - Actively leads Internal Safety Monitoring Committees (SMC) meetings (e.g., dose escalation safety meeting) & supports as needed. Provides input to safety charters Product Labeling, as Required for Work on Later Development Programs - Actively leads communication of CSC recommendations for labeling amendments, participates in Labeling Working Group meetings, leads communication of Safety outcomes to relevant stakeholders - Actively leads the development and maintenance of the Company Core Safety Information (CCSI), proposes edits and manages approval of amendments - Presents the CCSI to the labeling committee, contributes viewpoint to CCDS development, and reviews company core data sheet - Provides safety insights to development of Package Insert and Labeling Updates, develops labeling update impact summaries for use by RA, develops labeling prose text updates, based on internal aggregated reports Issues Management - Leads and manages escalation of potential issues to the SMT, ensures internal notification and provides updates - Leads and develops strategy for issue management and facilitates internal approval of plans - Leads the review of issue data and closure on recommendations, leads the drafting of an issue response document, reviews, and manages approval of issue response documentation and responses - Leads the formulation of a rapid response procedure, triage of potential issues to safety committee, executes Crisis Management response plan, reviews ongoing issue and plan - Reviews regulatory inquiry to lead strategizing the nature of response, best course of action and determines data specifications, Reviews relevant data required for response - Leads responses and contributes to formal response provided to regulatory agencies, reviews draft response, and manages approval of response - Actively leads the incorporation of latest updates and findings from ongoing pharmacovigilance and epidemiological analysis - Active