长沙招聘

Internship: Since September 2013; more than 6 months; ensure at least 3 days per intern every week.

Position Purpose:
1. Responsible for data entry of centralized protocol registration and NIS center registration
2. Support RQCA daily Quality Control (QC) report, such as help to run the study QC report
3. Support Quality Assurance (QA) activity, such as summarizing and analyzing QA results, and assisting in preparing the monthly QA summary.
4. Facilitate the training activities and RQC team meeting
5. Provide administrative support to Registry Quality Control Head, such as consolidating the performance tracking on a weekly basis, tracking and analyzing the metrics collection.

Qualifications:
2014 session of the graduate and undergraduate
Medical, Life Science, English majors, or other
Excellent English verbal and written communications skills, combined with outstanding listening skills
Strong teamwork spirit and good communication skills

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。