• 3-4年经验
  • 本科
  • 招1人
  • 11-09 发布
  • 五险一金
  • 通讯补贴
  • 定期体检
  • 专业培训
  • 年终奖金
  • 交通补贴
  • 免费班车

职位描述

职位描述: Position Purpose?Individuals filling the positions listed are responsible for one or more of the responsibilities as providing high quality, predictable and cost effective business analysis/support, standardized acquisition/divestiture execution, ad-hoc and scheduled data requests, safety aggregate report coordination, document formatting support, centralized SharePoint services support and value-added enabling shared services for the customers and solutions owned and managed by Information Management.?Primary Responsibilities?Provide support to plan and coordinate release of system changes and fixes, ensuring that business-side responsibilities are accounted for and completed, e.g., change management, communications, user acceptance testing, training material updates, training delivery, etc.?Supports utilization of IM systems and processes by responding promptly to end-user inquiries?Provide operational support to business for all In Reporting Service cross Safety, Clinical and Regulatory domains.?Develop and execute ad hoc or standard queries and follow established procedures to validate queries/results in support of business requirements?Manage and support BI and SQL queries developed for extraction and forecasting needs and provide metrics.?Provide analysis/consultant for the ideas of business process improvements/ innovations. Acting as SMEs to connect business stakeholders and BT to implement the solutions, including SharePoint, project tracking, auto scheduled report, etc.?Participate in developing and performing User Acceptance Testing (UAT) as required.?Gather metrics and generate standard reports regarding usage or support of IM systems?Liaise with WSR and DevOps business and technical groups to provide/review impact assessments 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.?Provide operationalized business support and services across DevOps and WSR domains.?Provide documentation support (e.g., format, link, version control etc.) to meet Pfizer’s standard and compliance requirements.?Continued improvement activities on identifying competitive operational services to release burden on the IM and business colleagues.?Contribute as appropriate to overall training program for IM systems and collaborate with business lines to ensure a consistent approach and minimal overlap with business process-specific training.?Complete training in accordance with Pfizer’s and DevOps COE Information Management curriculum.Technical Skill Requirements?Minimum of 3 years data management experience with clinical, safety, regulatory data and business processes in the pharmaceutical industry, including an understanding of the drug development process.?Knowledge of Clinical, Safety, Regulatory, and/or Document management systems and technologies?Experience with Microsoft word & excel, Adobe acrobat, ISI Toolbox, etc.??Strong capability on Project Management and Documentation?Experience on Business Object and Crystal Report (Optional)?Experience on Spotfire or Tableau?Experience on ETL/ Informatica?Experience with relational databases?Knowledge of application system management and change control processes, application validation and implementation in a GxP environment?Knowledge of Pharmaceutical metadata and standards?Experience with query tools/data extraction techniques (e.g., SQL, PL/SQL, Brio, MS_Access)Qualifications (i.e., preferred education, experience, attributes)?Bachelor’s Degree in life sciences, or 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. 职能类别: 临床数据分析员 信息技术经理/主管

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公司信息

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。

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