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Senior Medical Information Services Associate

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湖北-武汉 | 本科学历
2019-04-22 更新 被浏览:
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职位描述
性别要求:不限性别 工作职责:Role DescriptionCareer LadderPosition PurposeMISA is responsible for providing technical an d scientific support for designated Global Medical Information activities. These activities may include, but are not limited to information an d literature services, QA activities, inquiry fulfillment, peer reviewing, fact checking an d medical writing.Organizational RelationshipsReports to Head of GMI Wuhan reporting to Global Lead, Content Strategy an d Management in Worldwide Research an d DevelopmentPrimary Duties:Information an d Literature ServicesPerform 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 an d scope of requests to deliver high quality information an d reference services within agreed timelinesAnalyze, organize an d package literature search results an d information in summary formatMaintain knowledge of knowledge management resources an d information services/tools.Document-related ServicesCreate/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 mannerReview documents for content appropriateness, fact checking an d 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 an d therapeutic information an d disseminate as necessary/required.Inquiry HandlingSearch existing scientific database to appropriately answer an d process non-phone (e.g. electronically submitted) inquiries from customers an d fulfill inquiry requests via MI Global PlatformUnderstand an d comply with all applicable policies, guidelines, an d regulations related to the work being fulfilled (may be specific to Country of origin).任职资格:Training an d Education:BS, Masters, PhD degree in Life Sciences/Health Sciences Or related field, Or PharmD/MD/DOCurrent knowledge of standard medical writing guidelinesAdvanced knowledge of medical terminology.Experience with preparing an d conducting literature searches using various mediumsProficiency in the use of biomedical databases including Medline, EMbase, CoChrane Collaboration, MicromedexExperience with creating/developing written communications targeted at healthcare providers highly desiredProficiency in Microsoft Office packages an d familiarity with database management softwareKnowledge of Copyright Regulations an d Compliance preferred.Familiarity with AMA Manual of Style an d Electronic Document Management systems preferredSkill Requirements:Strong written an d oral English skills requiredAbility to summarize an d integrate large volumes of data into concise, but complete documentKnowledge of standard medical writing guidelinesStrong cognitive abilities, including verbal reasoning, attention to detail, critical thinking, an d analytical abilityThe ability to accurately track an d follow multiple versions of the same document during its revisionsAble to fact check science/medical content an d annotate references/slidesHigh level of attention to detail an d the ability to work in a concentration-intensive environmentCompetencies:Attention to detailIdentifies an d resolves errors an d discrepancies in study related documents. Notes an d resolves errors in written documentation.Communication, verbalConveys thoughts in a clear, concise, an d accurate manner. Uses correct grammar. Listens carefully an d asks questions when necessary to ensure understanding.Communication, writtenConveys findings in a clear, concise, an d accurate manner. Teleconference minutes an d agenda may require clarifications Or editions by project team initially, but patterns are not consistently repeated.Computer literacyUses required computer hardware an d software as productivity tools in performing work-related tasks. Enters information into company-required tracking programs with occasional outside assistance.Customer serviceDemonstrates professionalism an d presents a positive image of the company when called upon to interact with customers.Planning & organizingPrioritizes 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 makingSeeks input from others when faced with a difficult situation. Makes sound decisions within the scope of responsibility. Focuses on resolving problems.
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该公司的其他职位
  • 1000人以上
On October 31, 2005, Pfizer announced the official opening of China Research an d Development Center (CRDC) in Shanghai. Pfizer Global Research an d Development’s Center is mainly engaged in drug development activities. Much of the facility s capacity is devoted to the study design, data management an d 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 an d Risk Management an d covers the functions of safety data processing an d assessment. The center also trains Pfizer employees in China an d 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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