Clinical Data Coordinator

Review source documentation in CRIO and enter study-related data into sponsor EDC systems with high accuracy; verify data against source records to ensure completeness; identify missing or discrepant data and escalate as needed; maintain data-entry timelines and support data quality review and cleanup; follow SOPs, protocol requirements, and GCP guidelines; maintain confidentiality of patient and study information; communicate data status with study coordinators, data teams, and leadership; coordinate with U.S.-based clinical and regulatory teams to support multiple studies and sites; proficiency in Microsoft Office/Google Workspace and strong written/spoken English; ability to work independently in a remote setup; requires reliable high-speed internet and a professional remote work environment.