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Field
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orders in Maestro Care. May train or oversee others. Develops consent plans and documents for participants in a variety of studies. May train or oversee others. Develops and submits documentation for IRB
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Practice (GCP), IRB requirements, and human subject protections Experience using clinical research systems such as OnCore, eREG, iRIS, or electronic health records Experience supporting hematology, oncology
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point of contact for the OHSP offices, Email management, operational meeting agendas and minutes, administrative management of IRB membership, IRB account creation and trouble-shooting, paper and
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clinical course of research participants in clinical trials Coordinate with regulatory specialists and clinical trial coordinators and provide input related to IRB, DMSC, FDA and scientific review committee
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Level 43 Salary Range $19.56-31.29/hour Type of Position Staff Position Time Status Full-Time Required Education MS Click here for more information about equivalencies: https://hr.uky.edu/employment
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IRB Program Analyst - (26001251) Description Temple University's Research Administration Department is searching for an IRB Program Analyst! Become a part of the Temple family and you will have
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of operations and training materials; preparing, submitting, and maintaining IRB documentation; coordinating with domestic and international collaborators; and ensuring high protocol fidelity across study sites
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information about equivalencies: https://hr.uky.edu/employment/working-uk/equivalencies Required Related Experience 8 yrs Required License/Registration/Certification None Physical Requirements Sitting
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study status reports and maintaining study documentation. Submission of protocol, consent documents for IRB approval and assist in preparing regulatory submissions as requested Work at UF research
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Lexington, KY Grade Level 45 Salary Range $23.18-38.25/hour Type of Position Staff Position Time Status Full-Time Required Education BS Click here for more information about equivalencies: https://hr.uky.edu