Job responsibilities:
1. Responsible for comprehensive management of clinical research projects for medical devices:
2. Responsible for communicating and coordinating with data management personnel and biostatisticians, and obtaining seals for summary reports and clinical trial summary reports as planned;
3. During the project process, establish an internal training system for the project team to cultivate and enhance the work abilities of project members;
4. Responsible for the management of experimental instruments and internal cross departmental communication;
5. Assist superiors in completing other work tasks.

Job requirements:
1. Bachelor degree or above, major in clinical medicine, pharmacy or Biomedical engineering;
2. Have at least 5 years of CRA experience;
3. Possess excellent written and oral communication skills, be adept at active and positive communication, interact with various types of clients/researchers, and establish good relationships; Having excellent team organization skills and project management skills, such as organizing project team meetings, being able to quickly respond to problems and come up with solutions;
4. Possess service awareness and the potential to be customer-centric; Having the ability to work independently while also possessing a strong team spirit; Able to integrate and contribute to the team; Proficient in using computers and office software.