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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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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
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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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Excel, REDCap, SPSS, or similar software. Assist with IRB materials, protocol amendments, continuing reviews, and study documentation. Communicate with clinical, laboratory, community, and research teams
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Medicare coverage analysis, coordination of IRB or IACUC protocols, justifications. Understanding of post-award administration including set-up process, reconciliation, regular review, progress reports and
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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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Missouri University of Science and Technology | Rolla, Missouri | United States | about 18 hours ago
, assisting with study design, grant applications, IRB approval, data management, and manuscript preparation. Faculty and students collaborate on projects that advance the field of pediatric emergency medicine
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directly to life‑saving cancer research, this role offers deep exposure to FDA, IRB, and institutional processes while allowing you to grow as a subject‑matter expert in oncology clinical research. Minimum
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in team meetings. Participate in the development of complex documents such as protocols, informed consent forms and questionnaires, and complete IRB submissions. Show vigilance in patient safety and