1.Take the lead in building and maintaining internal and external cooperative relationships, link relevant parties such as clinical research centers, sponsors, CRO/CMO organizations, ethics committees and regulatory authorities, establish an efficient and smooth communication and cooperation mechanism, and resolve differences and difficulties in cooperation. 2. Lead cross-departmental collaboration, coordinate the company's internal medical, operation, quality, compliance and other teams, clarify the cooperation responsibilities and collaboration nodes of each department, promote the integration of cross-departmental resources, and ensure the smooth and efficient connection of all links in clinical trials. 3. Be responsible for staff training, carry out training related to internal and external collaboration in combination with core job responsibilities and clinical trial industry standards, and improve the professional quality and collaboration ability of the team and partners.

Educational Background 1. Bachelor's degree or above, major in Clinical Medicine, Pharmacy, Biomedical Engineering, Public Health or other related fields; master's degree or above is preferred. 2. Familiar with relevant laws and regulations in the clinical research industry (such as NMPA, FDA, ICH-GCP, etc.), and have a solid reserve of professional knowledge in the industry. Work Experience 1. 3-5 years or more of work experience related to clinical research; priority will be given to those with experience in internal and external collaboration and cross-departmental overall planning; priority will be given to those familiar with the docking processes of CRO/CMO, clinical research centers and regulatory authorities. 2. Have experience in team management and training, and have practical experience in independently establishing collaboration mechanisms and resolving cooperation differences. 3. Priority will be given to those with work experience in clinical research collaboration in the pharmaceutical and medical device fields; those who understand the entire clinical trial process will be given extra points.