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Dalian, China
Safety Operations Intern-DL
Internship
Health
Science
November 10, 2025
IQVIA
Life sciences analytics & research services
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Job Description
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
大连办公室:大连市高新园区腾飞软件园一期西翼10楼
*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。
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