Main work:
1. Assist researchers to complete the submission of ethical materials, the filing of pharmacological institutions and the signing of contracts; Assist to complete the safety report related to SAE and SUSAR in time;
2. Assist the researcher to complete the document collection, sorting and filing of the research center at all stages of the experiment;
3. Assist researchers to complete the management of subjects, including recruiting subjects, screening potential subjects, arranging subjects to visit, arranging laboratory tests and obtaining test results.
4. Assist researchers to complete the processing, preservation and transportation of test specimens;
5. Assist researchers to complete the management and inventory of clinical research drugs and related materials, including the receipt, preservation, distribution, recovery and return of drugs and related materials, and complete relevant records;
Education and professional background:
The lowest college education is mainly for some early practitioners, and now the mainstream is undergraduate education, with few masters and doctors. The major is medicine, pharmacy, nursing, biology and other related majors.