CRA for BE study/New drugs/Medical devices
1.Clinical research study setup/study procedure setup/site staff training
2.Site monitoring visits/source data verification/deviation reporting in compliance with GCP
3.Trial documents maintenance/regular site visits and maintenance/study materials supply/interim reports
4.regular report to sponsor/communication between sponsor and site.
5.site close-out/trial materials retrieval
6.audits/regulatory inspection participation upon request
1. Cell culture
2. Membrane-based and Cell-based functional assays
3. Radio-labeled assays and animal tissue extraction
4. New project or assay development, data analysis, literature review and search
5. Assay troubleshooting, optimization and validation
6. Equipment maintenance and SOP document system management
7. Brainstorming for innovative ideas on new assay method or new testing platform setup
8. Team support and other task assigned by supervisor