Job Responsibilities:
1. Design clinical trial;
2. Ensure that the design of the clinical trial program is expected;
3. Responsible for project allocation and supervision;
Job requirements:
1. Master of clinical medicine and above, will use statistical analysis related tools to give priority;
2. Have a complete experience in CRC or CRA, familiar with clinical trials and related policies and regulations;
3, willing to learn and challenge new things.
24 hours service hotline：