Clinical Research Coordinator

linicians, patients, administrators, auxiliary personnel, regulators, monitors, and sponsors; Understands and is knowledgeable of medical terminology, good clinical practice, FDA , OHRP , HIPAA policies; Experience with Microsoft Office Suite; Manages workflow independently with excellent organizational skills; Prioritizes quickly and appropriately with the ability to multi-task; Pays meticulous attention to detail Ability to review, understand, and apply complex protocols; Manages study materials including but not limited to, regulatory binders, study specific source documentation protocols training certification and other materials as required.