Medical Information Services Intern 武汉

月薪：

该公司所有职位
  • 无工作经验
  • 本科
  • 招若干人
  • 11-09 发布

职位描述

职位描述： Position PurposeA Medical Information (MI) Intern is responsible for providing technical and scientific support on MI documents review. The activities may majorly encircle the Fact Check Center, but also include (not limited) the other types, e.g., information and literature support, peer review, etc..Primary ResponsibilitiesDocument-related Support?Be responsible for reviewing the assigned MI documents.?Perform quality control on all response documents in GMI database. ?Demonstrate scientific understanding on content of response documents and references.?Ensure the overall quality of MI response documents by checking document accuracy, spelling and consistency based on the original researches/references.?Process documents in the MI database within specified timelines.?Communicate with responsible writers and reviewers as needed.?Communicate, escalate issues to project leader/supervisor.?Contribute to process improvements and additional special projects that may arise.Training and Education:?Junior or senior students / graduate students in Life Sciences/Health Sciences or related field, or the PharmD/MD/DO/DrPH candidates.?Proficiency in evaluation of published articles from trial design and statistic aspects.?Advanced knowledge of medical terminology.?Graduation in 2018 or later highly preferred.?Proficiency in Microsoft Office packages and familiarity with database management software.Skill Requirements:?Excellent English written and oral communication skills.?Basic knowledge of biostatistics preferred.?Ability to scan medical references and orient accurately and quickly for the information that need to be checked in the MI documents.?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 contents 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, writtenConveys 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. 职能类别： 生物工程/生物制药 临床数据分析员

联系方式

光谷生物城

公司信息

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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