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人才招募

和黄医药的目标是成为一家为中国和全球市场开发创新药物的领先的医药公司。我们诚邀有志人士加入我们的团队。我们致力于让每一名员工能够发挥才干,并提供互相协作的工作环境以回报您的才能和热情。如果您希望成为我们团队的一员,请将您的简历发送给我们

职能团队
临床及注册
临床开发
信息技术部
商业化
商务开发
生产
药物研究与发展
行政支持
工作地点
上海
中国其他地区
亚洲(中国外)
北京
欧洲
美国
苏州
香港
找到相关结果: 9
Key Responsibilities: Responsible for analyzing the market of HUTCHMED products and therapeutic areas. Analyze, coordinate and support the information needs of preparing new product launch; Formulate the of marketing strategy and roadmap from pr
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Key Responsibilities: Develop and execute market access strategies and commercialization plan aligned with country objectives; Work across functionally with global and local medical and commercial functions to develop value propositions and mess
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Key Responsibilities: Be the scientific expert on the assigned therapy area, disease area, clinical practice and competitor landscape; Handling pre-launching, providing professional medical advice in clinical aspect, and medical affairs activiti
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Responsibilities Prepare process R&D related documents and reports to support IND and NDA. Update technical documents and effectively communicate with process R&D team. Support process R&D team to provide documentation for IND, NDA, I
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工作职责 组织市场医学团队对于产品治疗方案相关文献的收集,国外文献检索翻译,产品资料的汇编,给予市场销售团队以医学支持与指导。 负责更新相关治疗领域最新的进展,为产品
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Primary Duties Management of clinical research project. Vendor (CRO, Lab, drug storage, etc.) supervision and management. Liaison with KOLs. Support IND and NDA filing. Quality control of the clinical research projects, such as co-monitoring. &n
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Primary Function The Statistical programmer/Senior Statistical Programmer is responsible for all statistical programming aspects at project level. The position is a key contributor with biostatistics in ensuring that pharmaceutical drug-developmen
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Responsibilities: High profile discovery-and-development toxicology leadership role for design, implementation, interpretation and reporting safety profiles for small molecule therapeutics, including IND- and Phase III-enabling toxicology studies
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Responsibilities Review product registration dossier and relevant documents Obtain IND & NDA approval as well as product registration license renewal as planed Coordinate with each function within HMPL from registration pathway Establish and
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