Clinical Trial Coordinator I

The Clinical Trial Coordinator I supports the clinical research team in ensuring studies are conducted in accordance with ICH GCP, applicable laws, SOPs, and protocols while managing study budgets and timelines. This role involves assisting with site identification, feasibility, start-up activities, document management, and communication with sites and regulatory bodies. The position requires collaboration with Project Managers, Clinical Research Associates, and the Study Start-up team to maintain compliance and drive study progress.