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Perform site selection (If applicable )), initiation, monitoring and close out visits in accordance with contractedscope of work and good clinical practice. P erform study start up activities, including site EC submission,contract negotiation, etc. If applicable, Clinical Research Associates may be accountable for development ofproject subject recruitment plan on a per site basis.
负责公司小分子创新药研发项目的管理
利用前瞻的技术优势,在高通量生物合成领域创造颠覆性的技术成果。
负责所承担项目的临床药理学和/或定量药理学研究/设计临床药理学研究并撰写I期研究方案和总结报告/与医学团队、早研团队等一起在项目组里推进临床项目。
根据公司立项和研发计划,制定公司产品注册年度计划并组织实施,主导整个申报注册过程,根据蕞新适用的法规,独立编制IND、NDA及变更等各类提交文件,跟踪项目审评审批及检验进度。
公司目前为了大规模生产,要在北京建设一个全新的工厂包括原液和制剂,2-3条2000升的产线,产品全球卖。目前公司诚聘生产副总裁,负责建设和管理新的工厂,同时管理目前的两家工厂,团队共计200人。
The job holder is responsible for the development of our client's operations in China. Key task areas will include but are not limited to market share improvement, financial performance, personnel development, physical asset management etc.This job is also open to expats who has solid working experience in China.
Report to the Board, comprehensively preside over the daily operation and management of the company. Achieve the company's listing goal.
Our client is a Family Business in Europe with Global Headquarter in China. Due to their business strategy change plus their full commitment in China, they are now looking for a Global CEO to join the organisation to oversee a 400 Million Euro business with around 3000 employees globally.
A U.S. company in the health-care industry is looking for a Senior Manager level compliance candidate to join their robust China business.
This role is China Head of Operation, directly report to China president. In charge of multiple plant operation management in China mainland.
创建职位订阅,通过电子邮件第一时间接收北京 生命科学 生物技术最新职位信息
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