北京市,上海市 | 若干人
• To collaborate 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 regulatory, business development, legal, etc.
• To maintain the highest standards of scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.
• To participate as a standing or ad hoc member in clinical study teams relevant to assigned molecule(s)/indication(s) and support the overall team with cross-functional integration, coordination and alignment to enable effective and efficient clinical development plan execution.
• To participate in ongoing clinical study meetings, including internal and external presentations, interactions and communications.
• To support and work closely with clinical study team in the development of study analytics, data management and safety profile in close-out clinical study activities to ensure correct medical/scientific data interpretation for interim and final study reporting.
• To work with ongoing data generation to address unmet medical needs and identify new or extended clinical development studies or other programs in the relevant therapeutic area of the assignment.
• To collaborate with relevant teams and other groups to measure and monitor study progress against objectives and plans, proactively identifies issues and challenges and comes up with potential strategic solution.
• To collaborate with relevant teams and other groups to convey clinical development perspectives and provide updates on strategies, plans and other activities.
• To assist the maintaining of in-depth knowledge of CFDA and worldwide drug-development regulations, national and ICH Good Clinical Practice (GCP) guidelines.
• Completes other special projects, as and when assigned, or otherwise requested.
📌 要求：硕士及以上学历，3年以上临床医生经验
🌟 优先：肿瘤药物研发背景，支持医学策略制定