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The UVA human subjects institutional review board (IRB) is accredited by the Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP) and as such can act as the IRB of record for multi-site investigator initiated trials; the UVA IRB also accepts National Cancer Institute (NCI) Central Institutional Review Board (CIRB) protocols.
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Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), Certified IRB Professional (CIP) or Certified IRB Manager (CIM) Conducts the preliminary preparation of IRB submissions to ensure completeness, compliance with administrative requirements, accuracy and scientific validity consistent with regulatory requirements and local policies.
$30.55 - $44.3 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Address development of IRB efficiencies, strategy, and policy within IRBMED, in alignment with Michigan Medicine, Medical School, and in association with the HRPP; collaborate within the HRPP infrastructure to develop and maintain consolidated IRB SOPs and assure the Operations Manual (OM) is congruent; develop and report metrics associated with IRBMED review activities.
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All human research studies carried out in the MRU are reviewed and approved by the Tufts Medical Campus Institutional Review Board (IRB). Bachelor’s degree in nutrition or Diet Technician, Registered (DTR.
$19.8 - $27.3 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Responsible for tracking projects including all study, investigator and Institutional Review Board (IRB) information, and patient. Actively collaborates with Research Programs related to protocol reviews, IRB submissions, and HIPAA compliance.
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Train on IACUC, IRB, EHS, Radiation safety protocolsComply with all applicable state, federal university, and sponsor policies and agreements. Train on IACUC, IRB, EHS, Radiation safety protocolsComply with all applicable state, federal university, and sponsor policies and agreements.
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The Regulatory Specialist will serve as liaison to investigators, collaborating divisions, departments and institutions, the Institutional Review Board (IRB) and external regulatory agencies. Ensures timeliness and accurate submission of all protocol amendments, ICF, Investigator Brochure and other administrative items to the IRB of record.
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The incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Oriented Teams (DOTs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors.
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Knowledge of human subject ethics and experience writing Institutional Review Board (IRB) research protocols. The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters.
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In addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted.
$48.32 - $88.16 an hourPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assist with non-financial award compliance such as IRB and IACUC approvals and monitoring program milestones. WPI thrives on innovative practice and welcomes diverse perspectives, insight, and people from diverse lived experiences, to enhance the community environment and propel the institution to the next level in a competitive, global marketplace.
$53,000 - $62,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Additional duties include support of FIT research activities, including data collection and entry, data cleaning, and assisting with Institutional Review Board (IRB) submissions, among other research related activities.
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They will lead policy and administrative support for the University-wide and College-specific committees that provide compliance reviews of research protocols, including IRB, IACUC, IBC, and College Human Subjects Review Committees.
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Ensure compliance with military-specific IRB regulations and guidelines. Develop a deep understanding of military-specific IRB restrictions, as well as effectively liaise with military units and command structures.
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Working under the very general supervision, and reporting to the Director of Operations, Anatomic Pathology and the Medical Director of Frozen Section,is responsible for managing the daily operations in the OR Frozen Section Room. Ensures that the necessary tissues for research protocols are obtained, without compromising the patient's diagnosis, according to approved IRB research protocols and in conjunction with the Tissue and Blood Biospecimen Repository.
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