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。
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。
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
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
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.