Description
CTI is hiring a Lead Clinical Research Associate to serve as the primary contact for assigned clinical trial study sites, conduct pre-study, initiation, interim monitoring, and close-out visits, manage site status and investigator communications, oversee investigational product and trial documentation, support regulatory and ethics submissions, coordinate with Clinical Data Management, mentor CRAs, and function as a Lead CRA for assigned projects. The role requires at least three years of clinical trial monitoring experience, a relevant bachelor's degree or equivalent qualification, hospital or pharmaceutical research experience, English fluency, and eligibility to work in Australia; it is a hybrid position in Sydney and does not offer visa sponsorship.
