Clinical Trial Operation Management: Establish working mechanisms and SOPs for clinical trial operation management to ensure that the progress of clinical trials meets the overall strategic requirements of each project and that the quality of clinical trials complies with the requirements of medical device quality management systems and regulations. Establishment and Maintenance of External Resources: Responsible for the management and maintenance of researchers, institutions, ethics committees, and CROs. Management and Evaluation of Internal Personnel: Based on the clinical trial needs of products under research, plan and establish working groups, reasonably allocate PM/CRA resources, and be responsible for the process management and result evaluation of clinical projects and working group members.

Master's degree or above in clinical medicine, pharmacy or other related majors, with English as a working language. More than 3 years of work experience in clinical trial project monitoring, with priority given to those with experience in clinical monitoring of orthopedic or implantable medical devices. Familiar with and understand overseas regulations and guidelines related to medical device research and development, registration and clinical research; proficient in the entire process of clinical research, able to organize and coordinate work at all stages, and good at continuously optimizing the clinical research process. Possess team management ability, good organizational coordination ability, pressure resistance, professional ethics and confidentiality awareness. Good at communication and with affability.