长沙招聘

Primary Requirements:
? Experience with business analysis in the Drug Safety area, with exposure to safety case data applications, capture and reporting processes is preferred.
? Demonstrated ability to perform a wide variety of business and technical liaison tasks.
? Experience with Oracle databases as well as Business Objects
? Experienced and skilled in querying from relational databases
? Familiarity/experience with support of Portal environments, including Microsoft SharePoint platform is preferred.
? Ability to interface with both customers and technical support to triage and resolve issues in a multi-application environment
? Negotiation skills with experience in a matrixed Team environment
? Experience with Microsoft products (e.g., InfoPath, Word, Excel, Access, Visio, Visual Studio) and query tools (Toad)
? Strong written and verbal communications skills
？ Self Starter with ability to work under minimal supervision.
？ Detail-oriented to ensure quality of work with minimal review.
Secondary Requirements:
？ Specific experience with commercial safety/clinical databases, e.g. ARGUS, ARISg is preferred.
？ Experience using SAS for data manipulation and analysis is preferred.
？ Experience with document management systems (Documentum)
？ Familiarity/experience with process-improvement methodologies and techniques
？ General knowledge of web-based server technology, architecture, language, and tools.

Primary responsibilities may include but are not limited to:
？ Provide operational support to business for all In Licensing and Divestiture needs for data migrations, Eg. generation of case lists and XMLs as required for divesting safety data. Managing forecasting and reporting by utilizing data from various systems (EP3, GRS etc) to provide accurate forecasts when data migration activity is triggered for In Licensing deals.
？ Manage and support BO queries developed for extraction and forecasting needs and provide metrics.

Secondary responsibilities may include but are not limited to:
？ Provide implementation services for projects in a collaborative model with the SIM INDI team, business and technology stakeholders. Services include requirements gathering, user acceptance testing, communications and change control.

？ Work with business and technical groups to provide impact assessments of business and technical change. Assessments to include the identification of affected processes and applications, required changes to these processes and applications, and alternatives to mitigate impact.

？ Support departmental portal projects and ongoing operation in a variety of roles. Includes facilitating requirements gathering and definition. Ability to drive business requirements into system change definitions. Provide cross-training for portal support where appropriate.

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。