长沙招聘

Zone / Line: Pfizer Medical, External Medical Communications (EMC) – Global Medical Information (GMI)
Reporting to: Group Lead of Group Lead of Medical Information Service
Location: BioLake, Wuhan

Position Purpose
• MISA is responsible for providing technical and scientific support for designated Global Medical Information activities. These activities may include, but are not limited to information and literature services, QA activities, inquiry fulfillment, peer reviewing, fact checking and medical writing.

Organizational Relationships
• Reports in to Pfizer Medical, External Medical Communications (EMC) – Global Medical Information (GMI)
• Responsible for liaising with relevant Global MI team members in support of GMI activities, as appropriate.
Primary Duties
Information and Literature Services
• Perform high quality searches of the medical literature in response to customer inquiries, or as it relates to creating/updating MI documents.
• Work closely with MI colleagues to evaluate the specific nature and scope of requests to deliver high quality information and reference services within agreed timelines
• Analyze, organize and package literature search results and information in summary format
• Maintain knowledge of knowledge management resources and information services/tools.

Document-related Services
• Create/update MI documents (e.g. Scientific Response Documents) in accordance with Global Style Guide (GSG)
• Summarize the findings from a search of the medical literature in a brief, but succinct manner
• Review documents for content appropriateness, fact checking and compliance with GSG.
• Perform QA/QC checks to ensure that data in documents are converted properly from the original version.
• Keep up-to-date with related product and therapeutic information and disseminate as necessary/required.

Inquiry Handling
• Search existing scientific database to appropriately answer and process non-phone (e.g. electronically submitted) inquiries from customers and fulfill inquiry requests via MI Global Platform
• Understand and comply with all applicable policies, guidelines, and regulations related to the work being fulfilled (may be specific to country of origin).

Training & Education Preferred
• BS, Masters, PhD degree in Life Sciences/Health Sciences or related field, or PharmD/MD/DO
• 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 Requirement
• Excellent English written and oral communication skills
• Japanese language skills, highly desirable
• 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

Competencies
• Attention to detail Identifies and resolves errors and discrepancies in study related documents. Notes and resolves errors in written documentation.
• Communication, verbal Conveys thoughts in a clear, concise, and accurate manner. Uses correct grammar. Listens carefully and asks questions when necessary to ensure understanding.
• Communication, written Conveys findings in a clear, concise, and accurate manner. Teleconference minutes and agenda may require clarifications or editions by project team initially, but patterns are not consistently repeated.
• Computer literacy Uses required computer hardware and software as productivity tools in performing work-related tasks. Enters information into company-required tracking programs with occasional outside assistance.
• Customer service Demonstrates professionalism and presents a positive image of the company when called upon to interact with customers.
• Planning & organizing Prioritizes time effectively based on work demands. Consistently meets timelines. Seeks management input with any difficulties in establishing priorities. Assists Study Manager in tracking compliance with study timelines.
• Problem solving & decision making Seeks input from others when faced with a difficult situation. Makes sound decisions within the scope of responsibility. Focuses on resolving problems.

简历接收邮箱：job-c2.china@pfizer.com

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。