- Support Data Management in Project Including but not limited: Verify the data according to the data validation plan, complete the data review on time, and query the suspicious data; Communicate with CRA in a timely manner to answer questions raised by the clinical site; Perform medical coding； Assist in designing and writing data management documents, such as data management plan, data validation plans, data transfer specification, eCRF entry guidelines, etc.; Participate in CRF UAT, edit check UAT and SAS listing UAT; Conduct reconciliation of serious adverse events； Conduct reconciliation of external data; Manage local lab normal range data; Prepare data review meeting data and materials; Implement data entry and consistency comparison according to project requirements; - Assist in Data Risk Management Including and not limited: Assist in developing Data Risk Management Plan and Data Risk Management Report/Listing, identifying potential risk, and following up risk mitigation action; - Communication & Problem Solving Communicate effectively with internal and external partners to solve data management problems in the project; - Data Support Provide data management support to other departments; - Other Other tasks that line manager assigns.

Education：Bachelor degree or above in clinical medicine, pharmacy, nursing, biostatistics, chemistry, biology or related fields; master degree is preferred. Work Experience：Fresh graduated Skills： English: Strong reading skills in English literature, as well as strong English writing skills. Computer: familiar with office software: word / excel / ppt Competency： -Good communication and cooperation skills; -Good analytical and problem solving skills; -Honesty and trustworthiness; -High sense of responsibility." Others Requirements：Travel frequency: about 5% of working time KEY PERFORMANCE INDICATORS -Accuracy Rate of Project Data -Compliance of Project -Timeliness of Project Milestones -Accuracy Rate of Database