找到相关结果： 9

业务经理

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

商业化, 香港 | 2021-03-25

外事务总监

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

商业化, 香港 | 2021-03-25

医学顾问

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

上海, 药物研究与发展 | 2020-05-21

副研究员/研究员，工艺研发

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

上海, 临床及注册 | 2020-05-11

市场医学经理

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�

上海, 临床及注册 | 2020-05-11

项目临床经理

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

上海, 临床及注册 | 2020-05-11

统计程序员

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

上海, 药物研究与发展 | 2020-05-11

毒理学总监

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

临床及注册, 临床开发, 北京 | 2020-05-11

高级注册经理

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