Job Openings at IQVIA in China - Page 2

职位概要 作为研究中心研究者团队的成员，在研究中心遵照研究方案、商定的工作范围、GCP、申办者/公 司SOP及其他相关指南和法规的要求，来协调和执行所分配的临床试验。 职责• 作为研究团队成员，遵照法规要求、商定的工作范围、适用的SOP、工...

Job OverviewProvide support to the Project Manager and related team members by performing routine procedures and tasks a...

主要职责1.根据试验方案、合同规定的工作范围、SOP和GCP的要求，协助CRA在研究中心进行简单的核查工作。2.协助CRA进行临床研究相关的文件整理工作。3. 完成直线经理和/或项目经理（PM）分配的其他工作。任职要求1.27届及以上在校生...

Responsibilities:Supports country SSU strategy in close collaboration with SSO Study Start-Up Team Lead and SSO Study St...

Job OverviewServe in support level capacity in CDM Validation (Testing) team, to perform testing activities in CDMS envi...

Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidan...

Job OverviewSecure and retain business through professional, consultative, proactive sales activities directed at decisi...

Job OverviewThe Global Alliance Management role is responsible for leading and strengthening strategic partnerships with...

• Supports country SSU strategy in close collaboration with the SSO Study Start-Up Team Lead and the SSO Study Start-Up ...

工作职责协助主管处理药品不良反应安全数据，包括：收集和跟踪传入的不良事件（AE）/终点信息、确定传入事件的初始/更新状态、跟踪事件处理完成的时间表等工作。 协助主管管理项目工作流程，包括数据库录入、质量控制活动和药品安全数据报告的生成，准备...