Job responsibilities:
1. Cooperate with clinical project managers and monitoring managers to implement domestic clinical projects:
(1) Based on the product clinical plan, determine the necessary information, key time points, and corresponding responsible persons for the project manager to implement clinical practice.
(2) Implement the clinical plan, control and implement the work at each node of the clinical trial process, start the clinical center on schedule, complete enrollment, follow-up, and close the center on schedule.
2. Responsible for daily communication and maintenance of clinical trial center institutions, ethics, and departments to ensure smooth trial progress.
3. Supplier management and supervision: Confirm that CRO and CRC carry out relevant work according to the contract.
4. Improve the workflow documents for domestic clinical trials.
5. Responsible for the management, verification, and warehousing of clinical unit trial samples.
6. Emergency handling and other tasks assigned by superiors.

Job requirements:
1. Bachelor degree or above, clinical medicine, Nursing, pharmacy or biomedical majors are preferred.
2. Relevant professional experience: at least 3 years; Experience in medical device and pharmaceutical CRA work is preferred; Experience in medical related fields is preferred.
3. Good English proficiency, strong reading and writing skills, CET-6 or above is preferred; Be good at communicating with others, have a good sense of service and strong adaptability.
4. Have strong teamwork spirit; Responsible, proactive, cautious and meticulous, with strong organization; Proficient in using various office software and equipment.