主要职责：

　　· 协助临床监查员/驻地监查员、项目启动部门在限定时间内，更新、保存、上传临床试验文件；

　　· 根据标准操作流程要求，协助项目组申请、保存、发放临床试验相关物资并保管相应产生的文件

　　· 协助项目经理和监查员在标准操作流程指导下完成临床试验文件的打印、复印、盖章等所需工作；

　　· 协助项目经理和监查员寻求供应商进行文件翻译、中心设备等器材的及时供应，协助财务和申办方在职责范围内进行物资结算和供应；

　　· 负责临床试验运营中各阶段财务材料的审核和付款，以及流程优化等。

　　· 协助项目经理准备项目会相关文件，完成会议纪要，维持临床项目团队的高效运营；

　　· 熟悉临床试验操作基本阶段和操作流程，及时反馈相关信息给临床项目团队。

　　职位要求：

　　· 全日制本科及以上学历；

　　· 细心、耐心、踏实、严谨的完成各项任务；

　　· 良好的学习能力和沟通能力，有效的时间管理和协调组织能力；

　　· 熟练使用Microsoft Word, Excel和PowerPoint；

　　· 英语读写熟练，口头表达流利，通过CET-6者优先考虑；

　　IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

　　IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

　　To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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