With over a year of experience in the clinical research field, specialized in conducting clinical trials for drugs and medical devices. Expertise extends across various trial phases, from pilot studies to phase I to phase IV. Worked in therapeutic areas such as chronic hepatitis B or D, drug-resistant epilepsy, respiratory syncytial virus, and myopia. Successfully conducted site initiation and provided interim monitoring to ensure compliance with ICH-GCP, SOPs, and regulatory requirements. Strengths include building strong relationships with site staff and sponsors, handling IRB submissions, and managing investigational products. Accelerated patient recruitment by fostering communication and resolving barriers with investigators and stakeholders. Possess strong organizational skills and flexibility, demonstrated through hosting sponsor visits, coordinating site tours, and presenting trial progress in English to international stakeholders. Fluent in English (proficient) and Mandarin (native).
TOEIC 910/990
Microsoft Office tools
Excel VBA
Python
Google Analytics
Digital marketing
Clinical data management