POSITION RESPONSIBILITIES

• Assist in planning and monitoring multicenter implementation of projects
• Assist in training and education of informatic tools in the ICU
• 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 avaiable and appropriate for the protocols
• Establish and maintain communication with professional and ancillary personnel
• Assist in IRB and other regulatory paperwork and administration
• Perform other related duties as assigned

QUALIFICATIONS

• 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

Minimum Salary Range

Maximum Salary Range

ABOUT US

Position

The Critical Care Study Coordinator will have responsibilities to support and assist the MD in administering and monitoring and daily operation of all critical care research projects. This position will be fully involved in all critical care studies and clinical trials, and will responsible for educating and training ICU staff on the division'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 sepsis, acute lung injury and other critical illnesses. 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, FDA and multicenter paperwork/interactions and other duties. Additional observational and/or therapeutic protocols are likely. SC must be willing to be flexible with the hours as needed for the study.