About The Role

Cross-Functional Team Membership & People Management Participates in the relevant Therapeutic Team (TT) Represents CD in Study Team relevant to assigned molecule(s)/indication(s) and helps ensure cross-functional integration, coordination and alignment to enable effective and efficient CD plan execution 2. Clinical Development Planning Stays abreast of internal and external developments, trends and other dynamics relevant to the work of CD to maintain, at all times, a fully current view and perspective of internal/external influences and/or implications for the assigned therapeutic and disease area(s) As appropriate, participates in competitive intelligence and/or other market/industry assessment activities and projects Maintains the highest standards and levels of scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment Collaborates with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in Clinical Development, research, business development, commercial operations, legal, etc. May participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input and guidance. Participates in CD strategy development and may present to various internal committees Supports CDL in creating and implementing the CD plan for assigned molecule(s)/indication(s) and/or other programs Supports CDL in the communication with HAs, as and when needed, or otherwise appropriate. Escalates matters, as needed, in a timely manner to his/her manager or other internal partners/stakeholders 3. Clinical Development Plan Implementation Supports CDL in the implementation of all relevant studies and programs: Participates in ongoing TT and relevant study team meetings, other interactions and communications Develops innovative clinical study designs for review and discussion with Medical Directors. Conduct appropriate literature searches Collaborate with clinical operations, other groups to develop consistent language and criteria for informed consent form ICF), protocol, case report forms (CRF), CRF instructions, etc. Reviews and/or writes additional medical documentation and/or provide medical input as requested or needed, e.g. protocol synopsis, safety monitoring plans, process documents, investigator brochures, or other relevant presentations or materials. Conducts ongoing reviews of medical/safety data Collaborates with clinical operations to develop and implement the overall data quality plan Consistently complies with, and ensures the same among relevant CST members, all governing laws, regulations, BeOne Standard Operating Procedures (SOPs) and other guidelines Qualification M.D. with relevant medical experience in Oncology area required. Academic/teaching background is a plus. Experience 2~5 years pharma/biotech industry experience OR is a recognized expert in the field 2~5 years experience with clinical trials, Oncology trials is a plus. Personal Competencies Fluent in English Good communication skills, both written and verbal Ability to travel globally ( 百济神州全球胜任力当我们通过以下十二项全球胜任力，展现出 "患者为先"、"无界协作"、"锐意创新 "和 "追求卓越 "的价值观时，我们就能帮助全世界更多患者获得更多负担得起的药品。 ●团队协作 ●提供并征求坦诚及可行的反馈 ●自我认知 ●兼容并蓄 ●积极主动 ●开拓精神 ●持续学习 ●拥抱变化 ●结果导向 ●分析性思维/数据分析 ●卓越财务 ●清晰沟通 BeOne Global Competencies When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. ●Fosters Teamwork ●Provides and Solicits Honest and Actionable Feedback ●Self-Awareness ●Acts Inclusively ●Demonstrates Initiative ●Entrepreneurial Mindset ●Continuous Learning ●Embraces Change ●Results-Oriented ●Analytical Thinking/Data Analysis ●Financial Excellence ●Communicates with Clarity 求职者隐私申明：百济神州致力于尊重和保护您的个人信息权利，并承诺依据合法、正当、必要和诚信的原则处理您的个人信息（包括个人敏感信息）。由于百济神州在全球范围内开展业务，我们可能需要基于人力资源管理等合理业务目的而将您的个人信息发送和/或存储在位于您所在国家以外其他国家（例如：美国）的服务器和数据库中，详情参见百济神州《求职者隐私政策》（百济神州官网 - 隐私政策 - 求职者隐私政策）。如您主动向我们提供您的简历信息或其他个人信息，则视为您已经充分理解并确认接受百济神州《求职者隐私政策》内容。如您对此有任何疑问的，请勿提交简历信息或其他个人信息。 BeOne is committed to respect and protect your personal information rights, and will process your personal information, including your sensitive personal information, based on the principles of legality, legitimacy, necessity, and integrity. 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Associate Medical Director, Oncology

About The Role