I have 6+ years of experience in clinical research, the most recent year in a biotech company where I am developing protocol on reconciling hard-copied correspondence in TMFs with electronic copies, providing support to clinical operations including preparation/shipment of study manuals, performing UAT and ordering CRFs. Additionally, I am conducting document reconcilliation on TMFs and cataloging TMFs using an excel tracker. My other 5 years have been working as a CRC for NIH funded studies.I have excellent interpersonal skills and very strong written and verbal communication skills; I am trilingual in English, Mandarin and Cantonese. I had experiences recruiting and consenting subjects, conducting interviews and following up with more than 500 patients in English and Chinese (Cantonese or Mandarin) which resulted in over 90% response rate. I hold my BA in Psychology from UC Berkeley and Certificate of Clinical Trials Design and Management from San Francisco State University.