1. Assist the project manager and clinical experts to complete the design of research scheme and other test data;

2. Be responsible for the investigation, screening, coordination, ethics review, agreement signing, supervision and quality control, recruitment progress supervision, follow-up and conclusion of clinical trial institutions;

3. Coordinate researchers, management institutions, CRC, sponsors, etc., and manage clinical trial affairs;

4. Data recovery and query resolution, assist in data management and statistical analysis;

5. Write the summary of the center and sign and seal the clinical trial documents;

6. During the training period with immature CRA skills, you need to work as a clinical research assistant (CTA)

1. Full time bachelor degree or above, major in medicine or related life sciences, fresh graduates or students without course tasks.

2. Be interested and enthusiastic in the clinical trial industry;

3. Understand relevant laws and regulations of clinical trials;

4. Those who have participated in formal GCP training are preferred;

5. Excellent academic performance and good English level;

6. Strong communication, understanding, analysis, induction, coordination, persuasion, organization and team spirit.