Clinical Research Coordinator

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered
by the non-cancer Clinical Trials Management Organization for Department of Emergency Medicine assists with assessing patient records to
identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains
informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and
families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments,
procedures, amp; other diagnostic testing in accordance with study protocol; participates in the collection, processing amp; evaluation of biological samples; administers questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and
notifies appropriate clinical professional to evaluate patient response, identify status of complications, amp; provide appropriate level of care;
documents unfavorable responses and notifies research sponsors amp; applicable regulatory agencies; participates in evaluating patients for
compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews
to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug
Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and
control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to
establishment of study goals to meet protocol requirements.