Clinical Research Coordinator
• Conduct independent and collaborative research analyzing disease trends and synthesizing information based on research objectives with work published in peer-reviewed journals• Manage and support all aspects of the regulatory process of clinical trials, including but not limited to preparing Institutional Review Board regulatory documents, patient data upkeep, communicating with sponsor monitors, and organizing site close out at the study close• Designed databases to capture crucial trial outcome data and progress tracking • Created workflows for research studies to most efficiently collect data for studies' endpoints• Coordinate with industry representatives to ensure expectations are met and exceeded while focusing on patient-care• Maintain patient contact throughout the trials through recruitment, obtain informed consent, scheduling patient visits, and clarify confusions or questions about the studies• Establish positive relationships with the patient and clinic staff while ensuring clear communication between the Principal Investigator, patient, and nurses • Train and supervise other research assistants
