SUMMARY OF QUALIFICATIONS:Experience analyzing Clinical Trial Protocols and the financial aspects of Clinical Contracts.Experience working with physicians, researchers, and other medical personnel in a research environment.Experience working as a Clinical Research Coordinator in hospital site.Thorough understanding of Good Clinical Practices, FDA, and ICH Guidelines, as well as hospital Internal Review Board regulations. Ability to liaison with surgical and image staff, as well as with representatives from pharmaceutical companies, equipment manufacturers, and academic institutions.Experience with web based eCRF system and IRB submission system, iMedRIS.Experience working in several cytogenetic and molecular biological laboratories.Self-motivated and detail-oriented with a strong desire to excel.Excellent written and verbal communication skills.Work successfully with individuals from different backgrounds and cultures.Proficient with Microsoft Office software. Fluent in both English and Chinese/Mandarin.
Listed skills include Molecular Biology, Clinical Trials, Clinical Research, Genetics, and 22 others.