• 2年经验
  • 本科
  • 招若干人
  • 11-09 发布

职位描述

职位描述: Position Purpose: The Information Analyst (IA) provides value added services in the collation, analysis and presentation of information to support key functions in the global Development Operations organization. These functions include but are not limited to: ? Providing basic or advanced analytics and modeling expertise to enable understanding of Pfizer’s clinical trial performances (quality, speed, cost) ? Developing and maintaining clear process models depicting clinical trial processes ? Tracking and reporting compliance with regulatory commitments or established SOPs/processes ? Providing operational support during the Significant Quality Event management cycle ? Maintaining training content for clinical trial staff and reporting compliance with training commitments Organizational Relationships: ? Reports to IA Supervisor or Lead in Wuhan Major Duties: - The major duties and responsibilities will include but are not limited to: Metrics & Analytics ? Collecting/extracting clinical trial related data or information (quality, speed, cost) from various sources ? Performing data analysis using various analytics tools, e.g. Excel, R, Python, SAS, Minitab ? Applying statistical methodology to conduct advanced data analysis, e.g. multivariate analysis ? Developing reports, scorecards or dashboards using various visualization tools (e.g. Spotfire, Tableau) that reflect clinical trial performances for various customers across the organization Process Modeling/Mapping ? Developing process diagrams for clinical trial processes and SOPs in the leading business process modeling solution - Casewise ? Maintaining process models via routine model publications and model patching in Casewise Quality & Compliance Assessment ? Accessing clinical trial related documentations in key systems ? Reviewing documents for content quality and /or compliance and comparing documents for consistent approach ? Tracking and summarizing data on findings Compliance Tracking ? Tracking completion of required activities by responsible parties across the organization ? Following-up with responsible individuals to o Remind/notify regarding actions needed, and timeframe for completion o Determine if follow-up has been completed by due date ? Maintaining information in tracking tool in a timely manner Training & Compliance Support ? Curriculum Administration ? Curriculum Reporting ? Course and Curricula Query Management ? Training Site Maintenance Education & Experience Preferred: Education: ? Bachelor’s degree or equivalent in statistics, mathematics, public health, epidemiology, computer science, engineering, biological sciences, etc. Advanced degree is desirable. Experience: ? 2+ years of related technical/business experience is preferred. ? Strong knowledge in multivariate analysis and skills in R, Python, etc. are desired. ? A solid understanding of the Microsoft Office suite, with advanced knowledge of Excel, is desired. ? History of achievement in a customer service role with demonstration of meeting customer needs and concerns. History of achievement in building strong customer relationships. Competencies: ? A readiness and ability to work to pre-defined standards ? Strong analytical skills ? Demonstrated effective communication skills ? Capability to communicate effectively in English, both verbally and written ? Must be accurate and have an excellent attention to detail and a quality control approach to work ? Ability to work effectively in a multi-cultural context ? Ability to work effectively in a matrix organization ? Utilizes and shares innovative approaches to build and maintain a competitive advantage ? Looks for opportunities for collaboration and acts upon them ? Respectfully challenges practices, decisions or ideas to uphold integrity and ethical standards ? Contributes to a learning organization, encouraging experimentation, risk-taking, and development in all aspects of work performance 职能类别: 系统分析员 临床数据分析员

联系方式

光谷生物城

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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