Description
CTI is hiring a Lead Clinical Research Associate to serve as the primary contact for assigned clinical study sites, conduct pre-study, initiation, interim monitoring, close-out, and remote monitoring visits, manage site status and study documents, support regulatory and contract activities, coordinate with Clinical Data Management, and mentor or train other CRAs. The role requires at least three years of clinical trial monitoring experience, a relevant bachelor's degree or equivalent qualification, hospital, pharmaceutical, or CRO research experience, English fluency, and eligibility to work in Brazil. It is office-based in São Paulo, with Spanish proficiency considered an asset and no visa sponsorship.
