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About the Role

The Critical Care Study Coordinator will support and assist the MD in the daily operation of critical care research projects. This role involves educating and training ICU staff, managing patient identification and interviews, and coordinating observational research studies and clinical trials in critical illnesses. The position will also oversee subject recruitment, sample collection, data collection and entry, and regulatory documentation.

Responsibilities

Support the planning, coordination, and monitoring of multicenter project implementation
Provide training and education on informatics tools within the ICU setting
Travel as needed to conduct site visits and deliver project-related training
Collect, manage, and accurately document research data and outcomes
Oversee study implementation at Montefiore and collaborating sites
Collaborate with research coordinators to ensure adequate study coverage
Lead patient screening and recruitment efforts
Perform data entry and maintain data integrity for ongoing projects
Ensure adherence to research protocols and study guidelines
Maintain organized and compliant clinical research records
Foster effective communication with clinical, professional, and ancillary staff
Assist with Institutional Review Board (IRB) submissions and regulatory documentation
Perform additional related duties as assigned

Requirements

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.
Clinical Research experience preferred
Bilingual (Spanish) preferred

Skills

Strong computer skills, including MS Excel.

Education Level

Bachelor’s Degree

Salary/Compensations

USD $58,500.00/Yr. - USD $58,500.00/Yr.