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documentation. Coordinate facility and equipment availability for study visits. Report adverse events, including serious AEs, to the IRB and sponsor. Document protocol deviations, reconcile test article
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documentation. Coordinate facility and equipment availability for study visits. Report adverse events, including serious AEs, to the IRB and sponsor. Document protocol deviations, reconcile test article
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for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu
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have experience coordinating clinical trials with all populations, including Hispanic and/or Native American communities. This includes completing IRB submissions (local and external), patient
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Coordinator - Sarver Heart Center Posting Number req26826 Department Sarver Heart Center Department Website Link https://heart.arizona.edu Location Tucson Campus Address 1501 N. Campbell Ave., Tucson, AZ
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(PI). 7. Attain and retain Clinical Research Coordinator Certification ( CCRC ). 8. Understand the process of preparing, submitting, and maintaining IRB , FDA , and/or other regulatory documents and
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, and oversight of research protocols, ensuring compliance with FDA regulations, GCP guidelines, IRB approvals, and HIPAA requirements. The CRC will collaborate with investigators, sponsors, and
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maintain accurate documentation. Coordinate facility and equipment availability for study visits. Report adverse events, including serious AEs, to the IRB and sponsor. Document protocol deviations
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pediatric oncology, hematology, hemophilia, and translational research trials. This position ensures full compliance with IRB/Human Research Review Committee (HRRC) requirements, Good Clinical Practice
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pediatric oncology, hematology, hemophilia, and translational research trials. This position ensures full compliance with IRB/Human Research Review Committee (HRRC) requirements, Good Clinical Practice