1. Implement the supervision of the clinical research center in charge according to the supervision plan;

2. Ensure that the clinical trials of the research center are carried out in strict accordance with the protocol, GCP and relevant laws and regulations, and protect the rights and interests of subjects;

3. Assist researchers in solving possible problems during the experiment;

4. Ensure that the research data are recorded in the case report in a timely, accurate and complete manner;

5. Collect, sort out and archive the research documents according to SOP;

6. Be able to undertake the work of project assistant and assist the project manager in quality control of clinical research;

7. Complete other related work assigned by PM manager.

1. Bachelor degree or above, major in medicine or related life sciences;

2. Have strong team spirit, communication and problem-solving ability, and be able to business travel;

3. Those who have participated in formal GCP training are preferred.