Nasdaq: $29.30 (+0.06) | AIM: £4.18 (-0.01)
人才招募

和黃醫藥的目標是成為一家為中國和全球市場開發創新藥物的領先的醫藥公司。我們誠邀有志人士加入我們的團隊。我們致力於讓每一名員工能夠發揮才幹,並提供互相協作的工作環境以回報您的才能和熱情。如果您希望成為我們團隊的一員,請將您的簡歷發送給我們

職能團隊
临床开发
信息技术部
商務開發
商業化
生產
臨床及註冊
臨床開發
藥物研究與發展
行政支持
資訊科技部
工作地點
上海
中國其他地區
亞洲(中國外)
北京
歐洲
歐洲
美國
蘇州
香港
找到相關結果: 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
閱讀更多
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
閱讀更多
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
閱讀更多
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
閱讀更多
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
閱讀更多
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
閱讀更多
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
閱讀更多
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.
閱讀更多
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
閱讀更多