Job responsibilities: 1. According to the GCP and company SOP to perform clinical monitoring work. 2. Ensure the test strictly according to the scheme, GCP and related laws and regulations. 3. Assist research center to solve possible problems in the experiment. 4. Ensure timely, accurate and complete research data recorded in a report on the case. 5. Report to project manager timely and comprehensive progress of the research center. 6. To assist researchers doubt timely completion data. 7. In a timely and complete research related to collect information. Benefits: five insurances, double cease, annual leave and bonus, insurance, etc.

1. Bachelor degree or above major in medicine 2. Knew generic companies or CRO company at least 1 years working experience 3. Have good flexibility, coordination and planning, good communication ability. 4. Able to adapt to business travel, compressive ability. 5. BE project experience is preferred.