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Field
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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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the operations of clinical, biomedical, and/or behavioral research studies involving human subjects • Coordinate study startup activities and communications with sponsors, local and central IRBs, and other key
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. Specifically, contributions towards analytic design and support. Assist with IRB and other regulatory requirements (e.g., data use agreements) Collaborate with multidisciplinary teams and stakeholders. May
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authorized by the IRB or institutional official. Conduct periodic compliance reviews of research protocols and documentation. Write reports and communicate findings with investigators, committees, and
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resource for investigators, supervisors, sponsors/CROs, IRB, ancillary departments, and institutional research partners; and may contribute to related start-up, data quality, coverage analysis, budget
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during course and at the close of the study. Represents the research program at meetings, national and international research consortia. Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other
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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
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clinical research team. Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Other duties as assigned. Performs all duties in accordance
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. Review IRB-approved protocols to ensure regulatory and operational compliance. Assist investigators and research teams with specimen-related research activities. Participate in cross-training opportunities
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Human Brain Imaging Research (CAHBIR; (https://sites.rutgers.edu/cahbir/ ). We seek candidates with expertise in network neuroscience, computational modeling, neuroimaging, and related approaches