Job Responsibilities：
1. Responsible for the organization and implementation of clinical trials projects of new drugs, including project arrangement, progress tracking, personnel arrangement, and reporting to the department director every week; 2. Responsible for clinical supervision, including writing clinical supervision plans, hospital screening, agreement negotiation, data handover and management, supervision and management throughout the clinical trials to ensure the smooth progress of clinical trials; 3. Assist in data management, examination, inquiry and statistical work, and assist in writing clinical reports; 4. Ensure that the clinical trial operation conforms to relevant laws and regulations and SOP requirements of the enterprise, and guarantee the trial process and quality control; 5. As the external liaison on behalf of the enterprise, coordinate and maintain the relationship with the participating units and personnel of the test project; 6. Manage the clinical operation team and be responsible for the work allocation, performance evaluation and development guidance of the CRA and CTA teams.
Job Qualification：
1. Bachelor degree or above (biological science, pharmacy or other health related disciplines), familiar with international and domestic technical guidelines and GCP standards related to clinical trials of new drugs; 2. Strong ability to analyze, summarize and write reports on experimental projects, as well as professional English reading and writing skills; 3. Strong communication and coordination skills, and a high level of professional dedication; 4. Over 5 years of clinical trial management experience and leukemia clinical trial background is preferred.
