KEY RESPONSIBILITIES（主要职责）

10. Maintain good relationship with key investigators

11. Maintain high standard compliance during the entire process

1. Bachelor’s Degree is required;

2. 5-year experience in clinical research with a minimum of 2-year experience of project management

3. Medical Device clinical operation experience is preferred;

4. Medical, Biology education or working experience background is preferred;

5. Demonstrated good knowledge of the NMPA regulations, ICH-GCP;

6. Good planning, organizing, team-work, leadership and communication skills;

7. Fluent skills in both spoken and written English

DESIRABLE（优先条件）

1. Experience of Class III products for endo-vascular therapies (e.g. stents), surgery registration clinical trials

2. Experience of NMPA inspection and audit;

3. Experience engaging and interacting with CMDE

Working conditions & environment(工作状况和条件):

(如是否需要经常出差? Home based?)

1. Business travel required. 30%

上班地址：中国上海市延安中路1228号静安嘉里中心