Clinical Research Coordinator
CurrentAssisted the Program Manager in planning and executing clinical studies, ensuring adherence to protocol standards, and driving process improvements.Provided support during subject enrollments by ensuring protocol compliance and ethical scientific standards. Off-site enrollments require preparing study documentation, verifying study equipment functionality, confirming data collection sheets are current and meet study protocol requirements. During off-site enrollment, provided support to team by administering questionnaires, maintaining adherence to research protocol standards, and reviewing data collection for quality assurance. Post-enrollment duties include securing and maintaining detailed study records of patient enrollment information and authenticating data collection for coding, and analysis of research data.Coordinated with Program Manager to ensure clinical research activities complied with federal regulations, hospital policies, and protocol procedures. Reviewed and comprehended study protocols to develop and prepare data collection processes, data cleansing, and establishing storage structures. Provided support to team members by developing training materials and tools for study personnel, allowing for task delegation between team members while maintaining protocol standards allowing for study timelines to be maintained. Worked with the Program Manager to manage day-to-day study activities, including problem-solving, communication, and protocol management. Attending investigator meetings as required and communicating time-line projections for studies. Collaborated with Program Manager to provide Principal Investigator with accurate reports of study updates. Collaborated with the Program Manager in the preparation of audit reviews by assisting with scientific and compliance reporting requirements as per federal regulations and agency policies.