Clinical Research Coordinator I

2 weeks ago


Tucson, United States University of Arizona Full time

Screen, recruit, and enroll participants for medical studies by
interviewing potential participants and reviewing medical history to
determine if eligibility requirements are met.Evaluate
potential study participants to ensure they meet eligibility
requirements, instruct study participants concerning research protocol,
and complete the patient informed consent procedure. Schedule
and/or perform medical testing per protocol such as drawing blood, vital
signs, EKGs, etc., includes processing and packaging of laboratory
samples for shipment.Assess participants during clinic visit;
perform initial review of study lab results; determine if patient is
experiencing side effects or other problems; and notify principal
investigator if problems arise. Complete case report forms for
each study participant and document medical data in the patient record
and sponsor database. Ensure case report forms or other data
collection/tracking tools are created if not provided by sponsor.Participate in sponsors site visits for assigned studies.Occasional out-of-state travel may be required for sponsor training.



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