长沙招聘

Position Purpose
Medical Information Services Intern is responsible for providing technical and scientific support to GMI Wuhan members. These activities may include, but are not limited to Information and Literature support, peer reviewing, fact checking activities.

the students who will graduate in 2015 or even later

Organizational Relationships
? Reports to GMI Wuhan Lead in Pfizer Medical, External Medical Communications (EMC) – Global Medical Information (GMI)
? Responsible for communicating with GMI Wuhan team members in support of GMI activities, as appropriate.

Primary Duties:
Information and Literature Support
? Perform high quality searches of the medical literature in response to the requests of GMI Wuhan team members within agreed timelines.
? Work closely with GMI Wuhan team members to create and maintain the search strategy pool for internal use
? Maintain knowledge of knowledge management resources and information services/tools.

Document-related Support
? Review MI documents (e.g. Scientific Response Documents) for fact checking and compliance with Global Style Guide (GSG) within agreed timelines.
? Provide internal support for summarizing articles, inserting product information or other support if neccesary

Training and Education:
? BS, Masters, PhD degree in Life Sciences/Health Sciences or related field, or PharmD/MD/DO
? Proficiency in evaluation of published articles from trial design and statistic aspects
? Experience with writing medical articles in English and current knowledge of standard medical writing guidelines
? Advanced knowledge of medical terminology.
? Experience with preparing and conducting literature searches using various mediums
? Proficiency in the use of biomedical databases including Medline, EMbase, Cochrane Collaboration, Micromedex
? Experience with creating/developing written communications targeted at healthcare providers highly desired
? Proficiency in Microsoft Office packages and familiarity with database management software
? Knowledge of Copyright Regulations and Compliance preferred.
? Familiarity with AMA Manual of Style and Electronic Document Management systems preferred

Skill Requirements:
? Excellent English written and oral communication skills
? Basic knowledge of biostatistics preferred
? Ability to summarize and integrate large volumes of data into concise, but complete document
? Knowledge of standard medical writing guidelines
? Strong cognitive abilities, including verbal reasoning, attention to detail, critical thinking, and analytical ability
? The ability to accurately track and follow multiple versions of the same document during its revisions
? Able to fact check science/medical content and annotate references/slides
? High level of attention to detail and the ability to work in a concentration-intensive environment

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。