长沙招聘

工作职责:

Responsibility

Accountable and responsible for the provision of standard and non-standard datasets, tables, listings and figures based on the protocol and SAP that are required for the study reports, submissions and product defense.

Serves as the point of contact and responsibility at the individual study level and may be responsible for multiple studies within or across assets.

Ensures excellence in the delivery of analysis ready data sets, tables, listings and figures, in order to advance research, development, and commercialization of the Pfizer portfolio.

Ensures adherence to high-quality programming standards in the production of clinical reports, and submission documentation.

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.

任职资格:

Qualification

With SAS/R/Python programming basic skill

Fast-learner, good team-player, good communication skill

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。