Job Description

该职位来源于猎聘 Main responsibilities:Deduce clinical trends, differentiations from clinical designs and clinical data read-outsMonitor and collect secondary information from a variety of sources, including clinical databases, such as Clinicaltrial.gov, the CDE, Informa etc., and article-based researchQuickly learn and work with sales and promotional data and Market and EpidemiologyAssessment, Pipeline Analysis and market research with senior supportAssist in data preparation, deliver components of projects, and help ensure excellence in final deliverablesDevelop a broad knowledge of consulting methodologies and the pharmaceutical market by delivering consulting services Role Requirements:Clinical related work experience is a MUST, welcome CRA, medical writer or clinical doctors with 2 years or above working experienceExperience on drafting, editing, or reviewing regulatory documents including clinical plan, protocols, CSRs, Investigator Brochures, and other regulatory submissionsExcellent ability in literature searching preferredWritten and spoken fluency in both English and MandarinProficiency in MS Word, Excel and PowerPointMaster’s degree or above; ideally in Medical, Pharmacy, Biopharmaceuticals, BiologicalSciences 职责描述:从临床试验设计或者数据中推演、总结趋势。独立搜集医药行业数据及资料、动态跟踪行业发展趋势。定期提交跟踪报告。跟踪不同治疗领域的动态信息,并分析数据确定关键发现和趋势, 形成初步报告。协助数据报告的准备工作并为项目成果高质量的最终交付提供支持。职位要求:熟悉临床试验的工作流程及相关法律法规。欢迎具有两年以上工作经验的CRA, medical writer和临床医生。参与或主导过临床伦理资料撰写、提交以及临床试验项目的资料收集、分析等经验尤佳。精通医学专业文献检索,并有较强的信息总结和资料撰写能力。具有信息敏感度和较强的热点捕捉能力,并有独到的行业见解。沟通能力强,具备敬业精神和责任心,有团队协作和大局意识。计算机网络检索技能,熟练使用Microsoft Word, Excel 以及PowerPoint。清晰的逻辑思维能力,高效的时间管理,项目管理能力。专注细节,有耐心。 学历要求:生命科学相关专业(临床医学、预防医学、护理学、药物学、生物学等)的硕士及以上学历 不论您是否有医药咨询的工作经验,只要您对咨询行业有颗热忱的心,公司不仅提供有竞争力的薪资福利,更为您提供系统的有针对性的培训,为您提供职业发展和自我提升的广阔平台!

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