长沙招聘

Coordinates / supervises all the tasks generated by clinical trials and which were entrusted to him/her by the Head of CPLs Ensures that these trials are carried out according to the required quality standard deadlines and to the CSU’s commitments. Represents a privileged link between the corporate team and the CSU within the framework of these clinical trials.
For clinical trials
-Support the assessment of the trial feasibility if applicable
-Makes a selection of investigators
-Prepares the file submission to the Ethical Committee
-Prepares the investigators’ contracts.
-Prepares the clinical trial AED
-Writes / validates the technical and/or administrative documents which are necessary for the trial and makes the Corporate documents fit the local regulations.
-Organises the local investigators meetings when appropriate.
-Ensures the good initiation of the centers, especially makes sure that the investigators are perfectly informed of the trial specificities and of its organisation.
-Ensures a good follow-up of the centers, i.e.
-By co-monitoring visits
-By assessing the monitoring reports
-By following the recruitment.
-Participates locally to the setting up of the audits carried out by the Corporate
coordinates the answers and follows up the possible correcting actions.
-Ensures an efficient liaison with designated IP support .
-Checks the payment of the investigators fees.
-Ensures that tolerance items are collected and reported.
-Makes sure that centers are properly closed :
-Files archiving
-IP and trial material collection.
-Keeps informed the investigators and the Health Authorities/ Ethical Committee of the trial’s results.
-Ensures the update of CTMS.
Clinical Study Unit
-Trains the CRAs to the study’s specificities.
-Coordinates the activity of the CRAs working on the study (centers allocation, workload)
职位要求：
-Cares for the implementation of the study’s instructions.
-Ensures the setting up of the study’s file inside the CSU.
-Informs the Head of CPLs of the progress of the trial and of the difficulties encountered, makes a review with him/her of the adequate strategy to be set up.
Corporate team
-Makes sure that the corporate team receives all required data on the trial progress.
-Participates in the meetings related to the trial and organised by the corporate team.

赛诺菲集团
赛诺菲集团是一家全球领先的多元化医药健康企业，专注于患者需求，传播健康。
 全球100,000余名员工，业务遍及100个国家
 新兴市场实力均衡，表现强劲，位列***
 多元领域，覆盖处方药、健康药业产品、疫苗和动物保健品
 疫苗领域的领导者
 领先动物保健市场
 2011年集团净销售额达334亿欧元

赛诺菲在中国
赛诺菲是首批在中国开设办事处的跨国制药集团，也是国内增长最快的医药健康企业之一。目前，赛诺菲在中国200多个城市拥有6000余名员工。
   
传承悠久历史、持续开拓进取
赛诺菲一直以来秉承对中国的承诺。1982年，赛诺菲成为首批在中国开设办事处的跨国制药企业之一。今天，赛诺菲已跻身中国医药健康市场的领军企业。赛诺菲的中国总部位于上海，并在北京、天津、沈阳、济南、上海、杭州、南京、武汉、成都、广州和乌鲁木齐共设11家区域办公室。

独特的医药健康产品系列、满足中国公共卫生需求
从预防到治疗，赛诺菲全方位满足中国的公共健康需求。集团的疫苗事业部赛诺菲巴斯德是中国领先的疫苗企业。赛诺菲在心血管/血栓、糖尿病、肿瘤、内科和中枢神经系统等关键的治疗领域拥有领先产品。2010年，杭州赛诺菲民生健康药业有限公司的成立标志着赛诺菲进入中国的非处方药市场。2011年2月，赛诺菲完成了对BMP太阳石的收购。

大幅投资工业建设、满足中国市场需求
赛诺菲目前在中国拥有六家生产基地，包括北京制药工厂、杭州制药工厂、杭州赛诺菲民生健康药业工厂、南昌梅里亚动物保健工厂、深圳赛诺菲巴斯德疫苗工厂、以及唐山健康药业工厂。

完善的研发架构、双赢的研发合作模式
在中国，赛诺菲具有从药物靶点发现到后期临床研究的整体研发实力。集团在上海设有中国研发中心和亚太研发中心，并在北京和成都分别设有研发机构。自2008年以来，赛诺菲与中国权威科研机构开展了10多项战略合作，在癌症、干细胞、糖尿病和老年疾病等前沿研究领域探索创新药物

依托于强劲的研发能力和多领域领先水平的广泛的医药产品资源，公司在中国的市场份额不断攀升，公司规模不断扩大，飞速发展的业务给了我们与更多优秀人才合作的机会。

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