Work content:

1, according to the relevant national laws and regulations, research programs, hospital and company SOP requirements, and with the authorization of the researcher, assist the researcher to complete various tasks.

2. Assist researchers to complete the submission of ethical data and filing materials of clinical trial institutions.

3. Assist researchers to complete safety reports related to SAE in time.

4. Assist the researcher to fill in the case report form, and complete the document collection, sorting and filing of the research center at all stages of the experiment.

5. Assist researchers to complete the screening, recruitment and follow-up of subjects, including recruiting subjects, screening potential subjects, arranging subjects to visit, arranging laboratory tests and obtaining test results.

6. Assist researchers to complete the management of clinical research drugs or devices and related materials, including receiving, storing, distributing, recycling and returning, and complete relevant records.

About China Resources

CRC is a clinical coordinator, which refers to the relevant transactional work authorized by the main researcher to assist the researcher to make non-medical judgments in clinical trials, and is the participant and coordinator of clinical trials.

CRC works mainly in free time, covering a wide range of cities and being relatively stable without traveling. After working 1-4 years, CRC experience and ability have been basically cultivated to a higher level.

If it continues to develop, it can be developed into a PM management project with more personnel, or it can be developed into a CRCLM to manage CRC and be responsible for CRC training and guidance.

Reference to the above content: Baidu Encyclopedia-Clinical Coordinator