Clinical Operations Director

1. Fully responsible for planning, implementing, operating, and managing clinical trial work; 2. Manage the clinical supervision team, responsible for team building and development; 3. Responsible for the entire process of clinical trials in research and development projects, including plan formulation, selection of clinical trial sites, effective project implementation, and quality control; 4. Participate in the development of clinical trial plans, including overall project progress plans, timelines, budgets, and manpower arrangements; 5. Track and inspect the completion status of each stage of the project, track the execution of experiments, promptly identify and solve problems, and ensure the quality and progress of experiments; 6. Responsible for communicating and exchanging key review experts, clinical experts, and other clinical research resources related to clinical research, assisting in developing correct clinical research strategies and plans, thereby ensuring the smooth progress of clinical research; 7. Responsible for summarizing and reviewing clinical trials, organizing clinical research meetings, and approving clinical trials; Responsible for managing and communicating to resolve issues related to conducting clinical research; 8. Responsible for the construction and training management system of clinical teams, establishing and regularly improving institutional processes related to clinical operations; 9. Provide necessary technical support related to clinical trials according to the company's development needs.