* Responsible for the development of clinical trial data management plan, assist in developing research programs and CRF table design
In charge of organization and management of clinical trials data entry, checking and finishing work;
* Clinical Trials Database for the establishment and management;
* Completion of clinical trial data for statistical analysis;
Complete the company assigned by the other data management related work, provide support
Requirements:
1. Biostatistics, preventive medicine and other related professional, master's or above;
2. Familiar with common computer software, including data entry of commonly used software, word, excel, powerpoint, etc., familiar with the network office, and various office equipment;
3. Work attitude, patience, and meticulous; strong sense of responsibility, a strong team spirit;
4. Good health, able to work under pressure;