- 工作职责
协助主管进行药品不良反应收集、统计、分析，及建立和保存药品不良反应监测档案等工作。 协助主管按照法规要求开展药品不良反应事件报告、定期安全性更新报告、事件调查、评价和处理等工作。
- 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，没有专业限制，具备生物、医药相关教育？背景为佳。 能够参加3个月以上的实习，每周至少可出勤3-4天，每个月至少出勤14天。
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.
