Job responsibilities:
1. Participate in the design and execution of clinical trials, as well as the review and analysis of subject clinical data;
2. Responsible for medical communication with researchers, research institutions, CROs, and regulatory agencies in clinical trial projects;
3. Manage and control the quality of clinical trials, and ensure that they comply with relevant regulatory requirements;
4. Be able to independently complete the Document retrieval, sorting and summary of Chinese and English academic articles;
5. Continuously tracking the latest progress in clinical research and treatment both domestically and internationally, and actively completing other work tasks delivered;

Job requirements:
1. Bachelor's degree or above in medicine, biology, pharmacy, or related majors;
2. Those who are familiar with the clinical trial process, able to independently carry out various coordination and related tasks, and have experience in writing clinical protocols are preferred;
3. Those who are familiar with the registration management measures for Class III medical devices, GCP regulations, and relevant regulations for clinical research are preferred;
4. Have good communication and teamwork skills, strong sense of responsibility, and work diligently and meticulously;