1. Implement the supervision of the clinical research center in charge according to the supervision plan;

2. Ensure that the clinical trials of the research center are carried out in strict accordance with the protocol, GCP and relevant laws and regulations, and protect the rights and interests of subjects;

3. Assist researchers in solving possible problems during the experiment;

4. Ensure that the research data are recorded in the case report in a timely, accurate and complete manner;

5. Collect, sort out and archive the research documents according to SOP;

6. Be able to undertake the work of project assistant and assist the project manager in quality control of clinical research;

7. Complete other related work assigned by PM manager.

1. Bachelor degree or above, major in medicine or related life sciences;

2. Have strong team spirit, communication and problem-solving ability, and be able to business travel;

3. Those who have participated in formal GCP training are preferred.

1. Assist the researcher to complete the management, recruitment and visit of subjects;

2. Assist researchers to complete the submission of ethical materials, and assist in the research and completion of SAE, AE and other relevant safety reports;

3. Assist in the data collection, sorting and archiving of clinical trial projects;

4. Assist in the management of device test and complete relevant records;

5. Assist researchers to cooperate with the central supervision of CRA and prepare various documents for CRA supervision in advance.

1. Nursing, pharmacy, clinical medicine and other related majors;

2. Clinical experience is preferred;

3. Strong independent working ability and teamwork spirit;

4. Have a sense of responsibility, positive and enterprising, cautious and meticulous, and strong organization.

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.