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redkey65

银虫 (小有名气)

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在线: 211.1小时
虫号: 667075
注册: 2008-12-03
性别: MM
专业: 中药学其他科学问题

[交流] 辉瑞武汉研发中心诚招临床试验助理（内部推荐）急招！

具体工作地点:

武汉光谷

薪金:

面议

学历和研究方向:

本科及以上，不限

招聘岗位:

临床试验助理

公司名称:

辉瑞（武汉）研究开发有限公司 / Pfizer (Wuhan) Research & Development Co., Ltd.

公司网址:

www.pfizer.com

联系方式:

redkey3@sina.com；

我们是这里，辉瑞武汉研发中心坐落于风景优美的光谷生物城，目前有500+员工。薪资福利等可百度了解。

我们在这里，我们是有风度也有温度的team，manager超级nice。近期业务扩张，还有5个空缺职位，急需人。欢迎各位踊跃自荐或推荐。

我们期待你，既读得了英文文献，又回复得了英文邮件。英文读写不成问题；看不太懂下面的职务描述没关系，我们有完善的培训机制来帮助你快速了解。

我们喜欢你，内向外向都ok，只要能静下心来做事情，喜欢笔记本办公模式即可，站着或坐着随意。其他的看眼缘吧，说不定我们就彼此看对眼签offer了呢。

工作类型：
正式员工 / Regular

联系方式:
redkey3@sina.com中英文简历均可

基本流程：
简历推荐---安排电话面试----笔试----发放offer（薪酬和入职时间）---正式入职

职务描述：
To provide operational and logistical support to global clinical trial programs in accordance with company SOPs, ICH GCP guidelines and local regulations.  To be the primary point of contact where responsibility is held as a Subject Matter Expert for a business system. •Provide protocol and ICD administrative support to global Project Managers (PMs) and Study Managers (SMs), including but not limited reviewing protocols, checking the consistency of documents, prepare RighTrack II protocol outputs report, circulate and track the approval status.
•Request set up of study team SharePoint spaces, grant access to the team and update files in SharePoint for Inspection Readiness documents including team roster changes, , updating version dates etc.,  and uploading of meeting minutes and any documents to SharePoint as required.
•Maintain Pfizer Trial Master File (PTMF) in accordance with ICH-GCP and SOPs.
•File documents to PTMF/ GDMS.
•Prepare and update the trial and site information as necessary in Corporate Clinical Trial Registry (CCTR) in a timely manner.
•Assist team with the preparation of any documents upon request, including but not limited to vender oversight plan, correspondence with investigator sites and vendors, study specific manuals for the sites, etc.
•Track and update all information on an ongoing basis per request, including but not limited to site contact information, required site training attendance, vender information, patient recruitment, trial suppliers, payment schedule, Ariba orders, etc.
•Attend appropriate training programs and project teleconferences as applicable.
•Support and coordinate any activities as requested by PMs/SMs and as assigned within required timelines.

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