长沙招聘

工作职责:

? Provide operational Reporting Service support to business on Safety domains.

? Develop and execute ad hoc or standard queries/reports and follow established procedures to validate queries/results based on business requirements

? Provide analysis/consultant for business requirement, give solution and implement the solution

? Participate in developing and performing User Acceptance Testing (UAT) as required.

? Provide documentation support (e.g., format, link, version control etc.) to meet Pfizer’s standard and compliance requirements.

? Participate in continued improvement activities on identifying competitive operational services to release burden on the IM and business colleagues.

? Complete training in accordance with Pfizer’s and GPD COE Information Management curriculum.

任职资格:

? Minimum of 3 years BI development experience. Candidates with Safety data and business processes in the pharmaceutical industry, including an understanding of the drug development process are preferred.

? Strong capability on Business Analysis, Project Management and Documentation

? Familiar with at least one BI reporting tool listed below. Experience on data model design, dashboard, report and analysis development, publishing, etc.

o SAP Business Objects

o Crystal Report

o Spotfire

o Tableau

? Familiar with Oracle databases

? Familiar with query tools/data extraction techniques (e.g., SQL, PL/SQL, SQL Plus)

? Familiar with Microsoft word & excel, Adobe acrobat, etc.

? Knowledge of Clinical, Safety, and Regulatory is preferred.

? Bachelor’s Degree in information management related discipline required.

? Knowledge of FDA, EMEA and ICH regulations is preferred.

? Demonstrated customer relationship skills and capabilities and collaboration on teams.

? Demonstrated ability to perform in a cross-functional environment.

? Strong verbal, written communication and presentation 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。