上海招聘需求分析师(IT方向)

需求分析师(IT方向)

辉瑞（中国）研究开发有限公司

公司规模：10000人以上
公司性质：外资(欧美)
公司行业：制药/生物工程

职位信息

发布日期：2019-05-16
工作地点：上海
招聘人数：若干人
工作经验：1年经验
学历要求：招若干人
语言要求：不限
职位类别：技术支持/维护工程师信息技术专员

职位描述

· Develop and execute ad hoc or standard queries to extract data from supported systems and follow established procedures to validate queries/results in support of business requirements

· Gather metrics and generate standard reports regarding usage or support of IM systems

· Investigates solutions to customer issues and develops or contributes to written materials that communicate solutions and/or options to relevant stakeholders resulting in appropriate decisions.

· Support continuous improvement projects to simplify and improve system use and system management.

· Participate in and lead small quality oriented projects intended to ensure high quality data in our regulatory tracking systems

· Provide data analysis support ongoing to key stakeholders for regulatory data

· Ensures that the company’s critical information and records stored within COE–owned repositories are managed in accordance with external regulations and internal processes, are protected and controlled over the long term and that content is available for critical business needs and is retained in accordance with established retention schedules.

Investigates solutions to customer issues and develops or contributes to written materials that communicate solutions and/or options to relevant stakeholders resulting in appropriate decisions

Technical Skill Requirements

· Experience with query tools/data extraction techniques (e.g., SQL, PL/SQL, Business Objects, Brio, MS_Access, VBA, Javascript)

· Demonstrated experience with systems management and maintenance including document management systems, databases, business process management and electronic workflow/routing tools, regulatory submission and tracking systems.

· General knowledge of web-based server technology, architecture, language, and tools.

· Experience with Microsoft Word, Excel, PowerPoint, Visio, project, Adobe acrobat, etc.

· Knowledge of Pharmaceutical metadata and standards

Qualifications

· Bachelor’s Degree in engineering, life sciences, information management, library science, information technology, computer science, business administration or related discipline required, master’s degree preferred.

Demonstrated, in depth knowledge of Pharmaceutical drug development environment and regulations.

· 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. Proficiency in Japanese is preferred.

· Ability to interact in a professional manner and build strong collaborative relationships with internal Pfizer teams.

· Ability to interface with international colleagues, understand the “big picture” in terms of potential implications of changes to systems and processes to sites and/or affiliates outside of home country/region

· Strong demonstrated project management and organizational skills

· Strong verbal, written communication and presentation skills.

职能类别：技术支持/维护工程师信息技术专员

公司介绍

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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