CRA临床监察员

招聘人数：9-10人 到岗时间：不限 年龄要求：不限 婚况要求：婚姻状况 1． 负责临床医疗器械产品的临床实验工作
In charge of the clinical trials during medical device trial period
2． 负责公司医疗器械临床试验现场的检查工作
In charge of the on-site inspection for medical device clinical trials
3． 负责医疗器械临床资料的组织、起草和整理归档工作。
Responsible for organizing medical device clinical data review, document drafting and filing work.
4． 负责协调研究单位和试验现场单位在临床试验过程中遇到的问题
Responsible for coordinating and solve the problem occurred in researching department and clinical trial center
5． 完成上级交办的其他工作
Complete other work assigned by superiors




1. 临床医学及相关专业本科或硕士学历，有临床工作经验者优先
Bachelor's or master's degree in clinical medicine and related, with clinical work experience is preferred;
2. 能独立处理常规的临床医学技术问题；
Have the ability to independently solve the routine technical problems of clinical medicine;
3. 良好的文献查阅、检索、总结能力
Good literature consult, retrieval and summarizing ability
4. 良好的表达能力、沟通能力、协调能力
Good interpretation, communication and coordination ability
5. 态度积极，有责任心，能适应出差
Positive attitude, responsibility, and can adapt to travel
6. 具有良好的英文表达能力和计算机水平
Good English skills and computer skills
7. 熟练使用微软应用程序包括word, power point及excel
Familiar with Microsoft software, including word, power point and excel;