长沙招聘

Required Experience:
? Demonstrated ability to perform a wide variety of business and technical liaison tasks.
? Experience with report developing, data modeling and ETL using Business Object.
? Skilled in querying from relational databases and be familiar with query tools (SQL, PL/SQL, Brio, MS_Access)
? Experience with Oracle databases
? Ability to interface/negotiate with both customers and technical support to triage and resolve issues in a multi-application environment
? Experience with well-defined System Life Cycle (SLC) environments
? Strong written and verbal English communications skills
? Detail-oriented to ensure quality of work under minimal supervision and with minimal review.
? 2+ years IT working experience is a must
? Degree from a recognized University
Preferred Experience:
? Pharmaceutical Industry, including experience with commercial safety/clinical databases, e.g. ARGUS, ARISg
? Exposure to Pharmaceutical data capture and regulatory reporting processes
? Coordination and management of User Acceptance Testing (UAT) modules
? Experience with document management systems
? Familiarity/experience with process-improvement methodologies and techniques
? Familiarity/experience with MS SharePoint/HTML
? Business analysis skills in the Pharmaceutical or Biomedical industry

Major Duties and Responsibilities:
? Liaise with business and technical groups to define or gather business requirements for data requests and reporting, define new business and support processes or improve existing processes.
? Perform data request activities, including Inspection related and standard data requests, ad hoc and custom reporting and data analysis services. Responsible for developing reports with business-specified formats, conducting system testing or peer review. Be able to deliver satisfied results with required timeline.
? Liaise with business and technical groups to provide/review impact assessments to reporting functionality of business requirements and technical change which include the identification of processes and applications, required changes to these processes and applications, and alternatives to mitigate impact.

Secondary Responsibilities:

? Preparation of clinical trial and safety data tables related to submissions. Contributions include, but are not limited to, NDAs, IND ARs and IIR Line Listing.
? Evaluates current systems and processes and actively offers suggestions for systems and process improvements.
? Promotes consistency and standards with internal processes and deliverables.

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。