武汉相关职位： 医药销售代表 医疗网络软件产品线总监(职位编号：20180003) 电话招商经理 UI设计师实习生 UI设计师助理 药品招商经理/OTC专员/销售代表 化工实验员 研发总监（食品安全快速检测） 全科医学研究员 高薪急聘医疗器械招商经理
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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无工作经验 -
招若干人 -
11-09 发布
职位描述
职位描述： Report to Programming TA Lead or Programming Team Lead Organizational Reporting Line Global Product Development (GPD)/Clinical Sciences & Operations (CSO)/Global Clinical Trial Execution (GCTE)/ /Development Operations China (DOC)/ Clinical Programming & Writing (CPW) Position Purpose • Accountable for the provision of standard and non-standard data sets, tables, listings and figures based on the protocol and SAP that are required for the study reports, submissions and product defense • Delivers according to the overall protocol timeline and quality goals through matrix communication within the Study Team • Ensures programming deliverables are reproducible, defendable and inspection ready at any time • Represents programming on study management team to communicate effectively within the teams and functional lines • Creates and maintains consistent, efficient and quality processes to meet timelines and deliverables • Champions operational excellence to provide continuous improvement of processes and sharing of best practices across TA’s 职能类别： 其他
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。
