1. Conduct screening, start-up, monitoring and closing visits of research centers in accordance with test protocols, SOP and GCP requirements.
2. Be able to supervise multiple research centers simultaneously.
3. Provide program and research-related training for the assigned research center, keep regular communication and address project requirements and issues with the center.
4. Assist in evaluating the quality and integrity of research center's work to ensure the compliance with protocols and regulations for clinical trials.
5. Provide constructive feedback on quality issues;
6. Manage the progress of the assigned research centers, follow up  the review and approval processes by clinical trial institutions/ethics committees, including subjects enrollment, completion and submission of CRF, and occurrence/resolution of data queries.
7. Develop/maintain documents related to research center management, inspection visits and action plans. Submit visit reports and other required research documents. 
8. Complete other tasks as assigned.
 

1. Bachelor's degree or above in clinical medicine, pharmacology, nursing, health management or other related field.
2. At least 2 years' experience in clinical monitoring,and GCP certification is required. CE project experience is preferred. 
3. Good oral/written English communication skills. CET6 level or above.
4. Good organizational/problem-solving abilities.
5. Effective time management skills, and being ability to handle conflicting priorities concurrently.
6. Able to establish and maintain effective communication relationships with colleagues and customers.
7. Adherence to SOP requirements at all times.