Job Responsibilities：
1. Participate in the clinical trial design, assist clinical managers to complete editing of clinical related documents such as CRF, ICF, recruitment materials.
2. Responsible for the research center, data preparation, submission; responsible for the communication and follow-up work of the project, the ethics, and the clinical agreement; the coordination, communication and treatment of problems in the central department of the project; responsible The experiment completed the research center closed.
3. Responsible for the quality of clinical project research.
4, track the progress of clinical project, coordinate CRO, researchers' clinical trials.
Qualifications：
1. Medical related majors, bachelor degree or above
2. After more than three years of drug clinical trial experience, participating in the clinical trial of the equipment is
3. Familiar with the national GCP regulations and have a good team spirit
4. Participate in one or more devices or clinical trials, familiar with the overall process of clinical trials
5, have a good English foundation, you can consult the English literature of the search project related products
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