1. Be responsible for reviewing the format of quality documents, as well as the management of quality documents and process management;

2. Update the quality control system in time and check the compliance of the center's quality system according to the requirements of clinical trials;

3. Be responsible for the quality control and management of clinical trials, conduct internal audit on clinical trials and issue reports;

4. Connect with the third-party audit company, review their audit plan and report, and follow up the implementation progress,

5. Review the responses of all CRA audit reports and track them until they are all resolved;

6. Regularly check the management of archived data by clinical trial assistants;

7. Assist in SOP training for new employees and prepare training materials.

1. Bachelor degree or above in pharmacy, medicine, law, etc;

2. Good document handling skills, good at communication;

3. Strong English literature reading ability;

4. Meticulous work, strong sense of responsibility, active learning.