Role at a glance
- Salary
- Not Disclosed
- Location
- Shanghai, China
- Work arrangement
- On-site
- Employment
- Full-time
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About the role
Original posting provided by Takeda
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Job Description
Qulifications 资质要求
1. 与业务部门合作,制定产品医学市场策略和 1-3 年的医学市场业务规划。
2. 洞察证据缺口,利用多元化证据生成支持产品科学价值故事以及生命周期管理
3. 提供产品和相关治疗领域跨职能部门的医学指导和支持。
4. 对公司产品组合的宣传材料进行医学审查,以确保从科学和伦理角度来提高品牌质量,对包装材料,包括包装内的药品说明书,进行医学审查。
5. 组织全国级别的非推广活动,包括专家咨询会和非推广性学术会议。
6. 评估和审核研究者提出的产品临床研究和医学教育资助申请。
7. 制定产品临床数据整合和出版计划,以在医学期刊上发表高质量的论文。
8. 发展与公司感兴趣的治疗领域中 KOLs 的高品质关系。
9. 向销售人员提供医学培训,回复专业知识查询
Qulifications 资质要求
教育背景: 临床医学相关硕士学历或以上
工作经验: 5 年以上医学院毕业后临床工作经验或有跨国制药公司医学事务工作经验者,资深医学顾问优先专业
技能:策略性思维、外部专家以及跨部门合作、英语听说读写能力熟练
Locations
Shanghai, ChinaWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeAbout the company
Takeda
Large Enterprise
Takeda is a global biopharmaceutical company headquartered in Tokyo, Japan, with a rich history spanning over 240 years. Specializing in the research, development, and commercialization of innovative medicines, Takeda focuses on therapeutic areas such as oncology, gastroenterology, neuroscience, and rare diseases. Committed to improving patient outcomes, the company harnesses advanced technologies and scientific expertise to deliver breakthrough therapies and enhance healthcare worldwide. Takeda's dedication to sustainability and social responsibility underscores its mission to strive towards better health for people and communities across the globe.