Phyllis Chan

A results-driven and diligent Clinical Operations Professional with extensive experience in trial management of global Phase I, II, and III trials from start-up to closeout. Demonstrated success in planning and implementing clinical trials, managing vendors/CROs, study document development, study monitoring, data review and reconciliation. Adept at leading collaborative teams and coordinating cross-functional study level activities to deliver high-quality data per FDA, ICH-GCP, SOPs, and protocol requirements. Experienced to successfully conduct large clinical studies in North America, Europe, and Asia-Pacific in rare diseases, renal diseases, and ophthalmological indications with small molecules and RNAi.