Clinical Research Coordinator
Current-Accurately and efficiently handle multiple IRB-approved Clinical Research Trials.-Facilitate pre-site selection procedures, study start-up, monitoring visits, and study closeouts.-Maintain seamless communication among sponsors, monitors, and vendors to ensure strict adherence to protocol compliance and site processes as per Standard Operating Procedures (SOPs).-Actively participate in patient recruitment, enrollment, and retention by disseminating protocols to healthcare providers, patients, and families, aiming to meet enrollment goals.-Complete data collection, source documentation, quality assurance, and regulatory submissions to ensure patient safety, study compliance, and progression.