The scope of responsibilities:

1. Adhere to the company rules and regulations;

2. Undertake daily administrative tasks for regional CRAs and assist line managers in their work;

3. Create folders for project files, communicate regularly with CRAs in the project team and organize the files for project centers as required;

4. Organize and coordinate meetings in the project team, manage the attendance sheets and produce meeting minutes;

5. Manage project files and strictly adhere to the NDA. Do not lose or leak any project file;

6. Coordinate and communicate with project team members and assist in completing project work;

7. Assist the project team to complete financial tasks in;

8. Help with writing/improving project-related charts;

9. Help with other tasks arranged by line managers.

Requirements:

1. Junior College degree or higher, fresh graduates are welcomed;

2. Proficient Office software skills and ability to organize files;

3. Basic ability to organize meetings;

4. Experience in positions related to clinical trials.