Responsibilities：

1. Participating in the preliminary preparations such as screening of clinical trial centers, design of CRF tables, preparation of ethical materials, and organization of researchers' meetings;  
2. In accordance with the protocol, GCP and company SOP requirements, start, monitor and end of clinical trials; 
3. Manage and address research related issues occurring at the study site;
4. Responsible for monitoring the quality of clinical research, tracking the progress of research and coordination of clinical trials, etc.;   
5. Assist the project director to complete the sample distribution and recycling, contract payment, summary report seal, etc.; 
6. Assist the project director to complete the work related to clinical research;   
7. Such as serious adverse events, should be timely and accurate report to the clinical manager;
8. Complete the other work arranged by the leader.

Eligibility：

Education/Major：	College degree or above in medicine, nursing or related field
Age：	25-35
Experience：	At least two years of experience in clinical trial supervision in the medical device industry
Knowledge：	Medicine、 nursing
Technical Ability：	1. Having experience in clinical trial supervision in the medical device industry and understanding the research and development of medical devices;   2. Have strong learning ability, can quickly accept new knowledge, work carefully, carefully;    3. Have good communication ability, can coordinate the relationship between the department (researchers), research base, the sponsor, properly handle the relevant matters.
Credentials：	/
Qualities：	Rigorous work, strong sense of responsibility, work enthusiasm, full of team spirit.