长沙招聘

? Participates in discussions with business partners to extract and document the requirements and critical business logic necessary for the data and reporting needs of the business lines.

? Participates in the delivery of aggregated data, reports, metrics, analytics and/or visualizations in support of business requirements, following established methodologies and processes.

? Conducts data analysis and investigations when issues with data are identified.

? Collaborates to define and implement information standards to ensure data integrity and quality across functions. Supports the compliance of information with internal policies and external regulations and standards.

? Proactively identify project and data issues and collaborate with the team to develop solutions

? Participate in Information Aggregation (e.g., Medical Data Cloud, Pfizer Operational Data Store) release activities, as needed

任职要求：

? Strong process, problem solving and analytical skills.

? Ability to explore, query and analyze various data sets

? Exposure to or experience in data analysis and visualization tools on both Windows and Linux/Unix systems (e.g., SQL, SAS, Business Objects, Spotfire, Tableau, Python, R, etc.)

? Exposure to data modeling, database design and ETL tools, desired

? Strong oral and written communication and interpersonal skills

? Understand Clinical, Safety, Regulatory and Content Management systems and processes

? Understanding and knowledge of tools and methodologies like:

o Methodologies: SDLC, Agile, SCRUM, BPRM, UML

o Testing Tools: ALM Quality Center

o Business/Data Modeling Tools: Microsoft Visio, SmartDraw, AnalytixDS

o ETL / OS: Informatica, Pipeline Pilot, Alteryx, SAS, Linux/Unix, Windows

o Programming Languages: SAS, SQL , R, Python

o Project Management: Microsoft Project, Microsoft Office

o Visualization Tools: Spotfire, Tableau, SAS, Excel

o Web Technologies: HTML, XML, JavaScript, SOAP

? Minimum Bachelor’s degree in information technology, mathematics, statistics or other relevant STEM program, or equivalent experience in scientific computing, computational sciences, bioinformatics or other relevant experience.

? Knowledge of project management, data analysis, business analysis, and information integration

? Familiarity with Clinical, Safety, Regulatory and Content Management systems and processes

Technical Skill Requirements

o Understanding of the drug development process, particularly clinical trial processes

o Experience using the following tools: Excel, Power Point, Business Objects, Spotfire, Pipeline Pilot, CAL / ODW and Activity Tracker.

o Knowledge of clinical trial and portfolio systems and databases

o High level of attention to detail, particularly in data entry and quality checks

Qualifications (i.e., preferred education, experience, attributes)

Education

o Bachelor’s degree or equivalent in biological sciences, health sciences, computer sciences, informatics, business, etc. Advanced degree is desirable.

Experience

o 2+ years of related technical/business experience is desirable

o A solid understanding of the Microsoft Office suite, with advanced knowledge of Excel, is preferred

o Experience with Visualization Tools, specifically Spotfire is preferred

o Experience with data processing and analysis techniques/tools (e.g. Pipeline Pilot, SQL, VBA) is desirable

o Excellent written communication skills required

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。