She started her career in clinical trials as a Clinical Trial Assistant and Study Drug Coordinator in 2005 and has been a Clinical Research Associate from 2006 until 2018. She has more than ten years of experience in the clinical research industry, both in multinational pharmaceutical companies and Contracts Research Organizations (CROs). She has been involved in clinical trial monitoring from Phase II to Phase IV, including study start-up activities and regulatory activities. She also has experience in monitoring overseas clinical research sites as country support in other Asia Pacific regions, including the Philippines and Malaysia.
Experiences in Therapeutic Area of Research:
