Job Description：

1. Assist the clinical research team in collecting, organizing, and archiving clinical research documents (TMF, etc.) and various reports, and implement primary quality control of trial documents;

2. Assist the project team in managing various costs, contracts, and related financial payment matters related to clinical trials;

3. Complete designated administrative tasks and provide support to team members in conducting clinical trials;

4. Assist the project manager in organizing project meetings and keep meeting records;

5. Assist CRA in preparing for experimental monitoring;

6. Complete other tasks assigned by the leader.

Job requirements：

1. Bachelor's degree or above in biology, pharmacology, or related fields;

2. Familiar with GCP; Good communication and collaboration skills;

3. Effective time management skills, as well as the ability to handle conflict work, proficient in operating and using software systems, with a certain level of stress resistance;

4. Positive and proactive personality, good communication and expression skills, and team spirit.