- 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，准备药品安全提交档案等工作。 其他主管指派的协助任务等。
- 任职要求
通过日语N2检定，或具备同等程度日语能力；并通过大学英语CET4级或以上。
学历要求为本科及以上，日语专业可，如具备生物、医药相关背景可优先考虑。
能够保证每周至少出勤24-32小时。
- 实习地点
合肥办公室：安徽省合肥市肥西县桃花镇明珠路与杭埠路交叉口西南角易商数码3幢
*接受远程和线下实习相结合的方式
- 顺利通过实习期考核即可优先得到正式offer。
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Top Skills
What We Do
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.
