1. Collect, analyze and organize clinical research progress and literature in this field in accordance with the company's product development requirements.

2. Assist in the drafting, writing and revision of clinical trial related documents, including clinical trial protocols, investigator manuals, ICF, CRF, project-specific forms, investigator training manuals, subject training manuals, research drug management manuals, etc.

3. Medical monitoring of clinical trials, collect and organize subject research data, and regularly summarize and provide summary reports for relevant discussions within the company or outside the research center.

4. Medical support for clinical trials, including answering questions from project teams and researchers.

5. Assist pharmacovigilance in making medical judgments on safety events such as AEs, SAEs, and SUSARs to ensure the safety of subjects.

6. Assist in drafting and writing clinical trial summary reports.

7. Assist in the maintenance and archiving of medical documents related to clinical trials.

8. Assist the head of the Medical Affairs Department in preparing training materials.

9. Complete other tasks assigned by the company's leaders in a timely manner.

1. Master of clinical medicine majoring in rheumatology and immunology, or a master of clinical medicine with research in rheumatology and immunology related topics;

2. Possess solid medical professional knowledge;

3. Possess proficient literature review, organization, and analysis skills, good logical thinking skills and copywriting skills;

4. Work meticulously, have a strong sense of responsibility, and have good learning ability.