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.本科及以上学历，医药相关专业优先，英语四级或以上。
2.表现优异并能够长期实习。
3.对临床研究和CRA有一定的了解。
4.每周可实习3天或以上（周一至周五），要求可尽快入职并能够至少实习3个月或以上。
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.