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The Study Coordinator supports the administration and daily operation of critical care research projects and clinical trials. Responsibilities include recruiting patients, managing data collection, and training ICU staff on study protocols.
Requirements summary
A Bachelor's degree is required, with experience in medical or public health research preferred. Candidates should possess strong computer skills and the ability to manage multiple priorities within a team environment.
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.
POSITION 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
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
Additional Information
In compliance with NYC's Pay Transparency Act, the annual base salary range for this position is listed below. Albert Einstein College of Medicine considers factors such as (but not limited to) scope and responsibilities of the position, candidate's work experience, education/training, key skills, internal peer equity, as well as, market and organizational considerations when extending an offer. Minimum
Salary Range
USD $58,500.00/Yr. Maximum
Salary Range
USD $58,500.00/Yr.
Bronx, New York
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