CRA team Intern 上海

月薪： 100元/天

该公司所有职位
  • 无工作经验
  • 本科
  • 招若干人
  • 11-09 发布
  • 专业培训
  • 弹性工作

职位描述

职位描述： Duties & Responsibilities？Apply, store, & distribute the stationery & commodities (include water, drinks, envelop, letter pad & name card etc.)？Support copy, print, file document etc？Coordinate & book meeting rooms in the company & send out the meeting invitations？Provide the admin supporting to investigator meeting events and activities？Collect and maintain the CRA/site/project related information？Provide logistic and administrative support to CRA teams.？CRA supporting:？Support CRA in tracking Safety reports (e.g. SUSAR and SAE) management at site level.？Support CRA in TMF document management, e.g. run the TMF completeness reports, overdue/past due report and TMF document timeliness report.？Support CRA in preparing the EC submission binder and site initiation package.？Support CRA in site level clinical trial expense management.？Support CRA in other activities, e.g. translation TMF documents.？ML supporting:？Support ML in tracking site level QCB metrics/CRA performance.？Support ML in other activities.Qualifications:？Bachelor or above background？Fluent written and oral English and Food knowledge of MS office？Good interpersonal skills？Strong sense of responsibility and a team work player 职能类别： 临床研究员

联系方式

公司信息

On October 31, 2005, Pfizer announced the official opening of China Research and Development Center (CRDC) in Shanghai. Pfizer Global Research and Development’s Center is mainly engaged in drug development activities. Much of the facility's capacity is devoted to the study design, data management and statistical analysis of global phase I-IV clinical trials, as well as the clinical study report process. In addition, CRDC is a part of Pfizer global Safety and Risk Management and covers the functions of safety data processing and assessment. The center also trains Pfizer employees in China and throughout the Asia region in internationally recognized Good Clinical Practice standards. 辉瑞公司于2005年10月31日宣布辉瑞中国研发中心正式在上海揭幕。辉瑞中国研发中心主要为全球辉瑞药物开发提供支持工作。大部分的功能是围绕在I-IV期临床试验研究设计、数据管理和生物统计分析、以及临床试验报告的部分准备工作。此外，该中心是辉瑞全球安全和风险管理部的一个分支，负责安全数据处理和评估工作。研发中心还将为辉瑞公司在中国及亚洲的其它运营部门的员工提供国际标准的临床试验管理规范(GCP)的技术培训。

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