药品注册主管 经理RA supervisor Manager—北京

目前我们正受世界知名制药公司的委托，在全国紧急寻找以下职位（上海，北京，广州，杭州）：CRA/主管/经理， 医学信息专员/主管/经理，药物安全专员/主管/经理，医学经理，注册经理（北京），注册专员。如果您符合以下的背景，请发送您的简历至edwin_hong@fmces.com, 我们会尽快与您联系。把握机会，我们会给您一个惊喜。 药品注册主管/经理RA supervisor/Manager—北京
Responsibilities:
Specific tasks:
- Regulatory Affairs
- Ensure regulatory integrity and timely delivery of quality registration dossiers.
- Initiate dossier preparation, request available regulatory documents from HQ and within
China (Scientific Affair, Clinical Affair, and Tech Op)
- Oversee all communications with Drug Registration Authority, including samples submission,
import related regulatory issues, clinical trial application, market authorization and production authorization.
- Evaluate regulations, establish framework, design and implement science based registration
- Provide up-to-date regulatory intelligence.
- Establish departmental SOP

联系我们时，请说明是在职友集看到的，谢谢！

发布时间：

2010-04-21

来源网站：

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