Study Coordinator

• Assist in planning and monitoring multicenter implementation of projects
• Assist in training and education of informatic tools
• Assist in outreach and coordination of Community Advisory Board activities
• Travel if necessary for site visits and training for projects
• Collect and accurately record data and outcomes for research and monitoring
• Manage study implementation at Montefiore and other sites
• Coordinate efforts with other research coordinators at Montefiore to be able to provide study coverage as needed
• Oversee patient screening and recruitment
• Perform data entry for ongoing projects
• Ensure implementation of research protocols
• Ensure clinic research records are available and appropriate for the protocols
• Establish and maintain communication with professional and ancillary personnel

• Bachelor’s Degree required.
• Experience in medical or public health research is preferred.
• Ability to manage multiple priorities and projects while working as part of a team.
• Strong computer skills, including MS Excel.
• Clinical Research experience preferred
• Bilingual (Spanish) preferred

Position

The Bioethics Critical Care Study Coordinator will have responsibilities to support and assist the Director in administering and monitoring and daily operation of all Bioethics Critical Care research projects. This position will be fully involved in all Bioethics Critical Care studies and clinical trials, and will responsible for educating and training Bioethics Critical Care staff on the Center's studies, protocol and importance; manage mechanisms for identifying eligible patients and their surrogates; manage subject interviews; initiate, manage, and coordinate several observational research studies and clinical trials in racial and ethnic disparities in quality of serious illness communication and care. The Bioethics Center uses Community Based Participatory Research methods to partner with African American/Black and other minoritized communities in the Bronx to improve healthcare communication and quality. The position will also oversee subject recruitment, interviews, sample collection and processing, training of research and clinical staff, monitoring/reporting of research compliance and adverse events, data collection and entry, multicenter paperwork/interactions and other duties. Additional observational and/or trial protocols are likely. SC must be willing to be flexible with the hours as needed for the study.