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Clinical Research Coordinator
This position is responsible for screening and recruitment of study subjects of patients who are hospitalized. Schedules and completes study visits based on protocols, data entry, and monitoring of study compliance relating to the human subjects committee, the federal government, and study sponsors. Other responsibilities include working with nursing staff and physicians to ensure protocol compliance, obtaining research specimens for laboratory analysis, reviewing patient charts for collecting data for prospective and retrospective studies. Specific duties include: Subject screening and recruitment Schedule and complete study appointments with subjects based on study protocol Accurate and efficient data accrual and case report form


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