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assistance to support their thesis projects. The full job description is here: https://www.dropbox.com/scl/fi/to4moi200ahe3ul6lj814/TA1_Seethapathi_083126.pdf?rlkey=abg7tj181gflnaxn31w4pmdne&st=jjmu0qd4&dl=0
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physician-scientists, cares 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
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Details Posted: Unknown Location: Salary: Summary: Summary here. Details Posted: 01-Jul-26 Location: New York, New York Type: Full-time Categories: Grants Management Internal Number: 285533308 IRB
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research methodology Maintain complete, accurate, legible records. Thoroughly document any modifications. Manage Research Activities (10%) Write and maintain IRB protocols, deadlines and approvals
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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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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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Coordinator II. The Clinical Research Regulatory Coordinator II will prepare, submit, and assist with multiple levels of research documentation, IRB submissions to UAB, WIRB, Advarra, and others. Maintain
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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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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