长沙招聘

职位描述：

Position Purpose

Individual filling this position is responsible for providing execution/delivery in support of alignment of Information Management data domains into authoritative information solutions and services. Incumbent will work closely with the Lead to manage the solutions, services, and standards for information integration and aggregation will also participate in the implementation of data standards and data stewardship across functions.

Primary Responsibilities

? Helps define and implement information standards (includes multiple standards, e.g. reporting and storage standards, master data, etc.) to ensure integrity and stewardship across functions

? Assists in gathering and documenting information requirements and working with the business to define standards and rules to ensure information is compliant with internal policies and external regulations

? Assists in profiling information as identified in business requirements

? Assists with the development of regulated and operational reports

? Ensures Integration and Reporting Platforms are fully compliant and inspection ready

? Partners with Business Technology on Change, Release and Problem management for the systems portfolio

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

? Responsible for the business activities supporting implementation

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

? Ensure all activities comply with IM procedures, global regulatory requirements and SOPs

Technical Skill Requirements

? Excellent analytical skills with demonstrated ability to investigate and solve problems

? Technical background with demonstrated skills in data analysis and visualization tools on both Windows and Linux/Unix systems (e.g., SQL, SAS, Business Objects, Spotfire, Tableau, Python, R, etc.)

? Experience in 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:

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

- Testing Tools: ALM Quality Center

- Business/Data Modeling Tools: Microsoft Visio, SMARTDRAW, Analytix DS

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

- Programming Languages: SAS, SQL , R, Python

- Project Management: Microsoft Project, Microsoft Office

- Visualization Tools: Spotfire, Tableau, SAS, Excel

- Web Technologies HTML, XML, JavaScript, SOAP

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

? Minimum Bachelor’s degree in life sciences, business, engineering, statistics or a related discipline with a comprehensive understanding of data and systems used in the R&D processes.

? Must possess knowledge in project management, data analysis, business analysis, and information integration

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

? Experience working with international colleagues, with demonstrated facility to understand the “big picture” in terms of potential implications

? Strong demonstrated project management and organizational skills.

? Demonstrated customer relationship skills and capabilities and collaboration on teams.

? Strong verbal, written communication and presentation skills.

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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。