上海相关职位: 临床协调员(CRC) 项目经理(PM) 高级临床协调员(CRC) CRC主管 合成肽生产技术员 类病毒颗粒(VLP)疫苗研发工程师 研发工程师(体外诊断生化产品) (职位编号:001) 医药代表(上海) 大客户销售 Clinical support (临床支持)
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
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本科
招若干人
11-09 发布
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
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。
医学专员 1-1.5万/月
细胞治疗临床研究主管 6-8千/月
临床销售代表(浙江、杭州) 4-8千/月
医药销售代表 1-1.5万/月
工艺研究员 0.8-1万/月
注册总监或高级注册总监(兼首席注册助理) 30-80万/年
频道医学编辑 6-9千/月
实验室发货专员 3.5-4.5千/月
慢病毒包装技术员 3.5-5千/月
高薪急聘慢病毒包装技术员 4-6千/月
报告撰写专员(实习生亦可) 3-4.5千/月
合同评审及风险管理专员 4.5-6千/月
上海相关职位: 临床协调员(CRC) 项目经理(PM) 高级临床协调员(CRC) CRC主管 合成肽生产技术员 类病毒颗粒(VLP)疫苗研发工程师 研发工程师(体外诊断生化产品) (职位编号:001) 医药代表(上海) 大客户销售 Clinical support (临床支持)
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
