上海相关职位： 质量保证工程师（QA，抗体中心） 质量工程师 Drug Safety Associate/Pharmacovigilance Specialist 微生物研发人员 研发工程师（分子生物学） 生物测序 生物检测技术员 高级验证工程师 质量检验员/QC RA Specialist/器械注册
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 -
本科 -
招若干人 -
11-09 发布
职位描述
职位描述： Job Responsibility:Work with clinical study team to interpret study results and prepare Clinical Study Reports (CSRs) and related documents.Requirements:Graduating in 2017 or 2018 with a Bachelor’s or Master’s degree preferably in medicalsciences or life sciencesHighly motivated, responsible and quick learnerExcellent verbal and written English language skillsAttention to factual detail and accuracyComply with company policy and uphold the highest level of integrityAbility to work effectively in a multi-cultural contextExcellent interpersonal and team-working skillsAssertive with good influencing skillsBasic knowledge of using Windows OS, MS-Word, MS-Excel, E-Mail (MS-Outlook)Able to work 3 or more days a weekDuration of internship: 6-12 monthsLocation: ShanghaiContact info: Please send your electronic CV (both Chinese and English), academic transcript and award certificate to ChinaCPWTalent@Pfizer.com 职能类别： 生物工程/生物制药
联系方式
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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。
