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The position is highly strategic and responsible for:
A U.S health Company is looking for a Senior Ethics & Compliance Manager to join their Beijing office.
A U.S. medical device company is looking for a senior legal counsel to join their Legal team in Beijing.美资医疗器械公司诚招一名高级法律顾问。
Looking for an FP&A specialist with 5-year experiences in finance, open to candidates with accounting background and good potential
国内知名大型医疗集团诚招一名了解有医药行业背景的战略总监。
Immediately available candidates with at least 1-2 years of experiences in customer operation OR order management are preferred
CEO汇报给董事会,负责公司全面的运营管理。
纳斯达克上市国内生物科技企业诚招一名法务负责人。汇报CEO。
A fast-growing European pharmaceutical company is looking for a legal counsel/senior legal counsel (Sole Counsel) to join their China team. This role is based in Beijing.
The Network Operations Engineer is a member of Digital Technology's Global Network Service Team. The Engineer is responsible for running the network environment in its intended state which includes maintenance, troubleshooting, and repair of the Global Network. The Engineer also provisions service requests such as firewall changes and other common requests
我们的客户是一家有全球化视野的创新药公司,产品管线丰富,管理团队背景优秀,已经登录资本市场。因业务发展需要,招聘一位内控总监,优秀的英文能力。
A U.S. company in the health-care industry is looking for a Senior Manager level compliance candidate to join their robust China business.
纳斯达克&港交所双上市,扶持赛道发展空间大;薪资待遇优越,可以即刻上岗;
The aim of this regional role is to embrace an entire region with regards to all risk management and internal control system topics. Engage deeply with the CFOs of the different entities to develop and implement risk management & internal control system. Ensure the transparency of the entire risk situation, making sure that the local risk assessment processes are performed thoroughly and risk mitigating strategies are implemented and followed up in time.
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。
根据产品注册进度要求,组织协调、督导各部门工作进度,保障申报资料的汇编按时完成;指导注册人员开展相关品种的注册申报,推进已申报品种的注册进度;
产品呼吸机;硬件软件研发总监,lead几十人的团队。
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.
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