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Provides oversight and guidance for the Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and Health and Safety Committee. Manager, Academic and Research Operations; Specialist, Grants and Contracts, IRB Chairperson.
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Oversees research activities by coordinating Institutional Review Board (IRB) approved research studies with the Pathology Research Coordinator ensuring research requests are completed and billed properly.
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Working Title: The (IRB) Institutional Review Board and Sponsored Research Specialist. Bachelor's degree in a field relevant to research compliance or research administration, and experience in research administration, regulatory compliance or Institutional Review Board (IRB)/human subjects protection administration, or an equivalent combination of education and experience.
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Prepares IRB/IACUC/radiation safety/bio hazard compliance documents and oversees maintenance of regulatory documents, files, and reports. Prepares IRB/IACUC/radiation safety/bio hazard compliance documents and oversees maintenance of regulatory documents, files, and reports.
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Research across Atrium Health is coordinated by the Wake Forest University School of Medicine Clinical and Translational Science Institute, which operates under a single IRB and contracts office, facilitating clinical trial execution and research integration in multiple markets.
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Providing nursing research support for IRB and Institutional Animal Care and Utilization Committee (IACUC) approved research protocols. Experience supporting research protocols for IRB and Institutional Animal Care and Utilization Committee (IACUC.
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Serves as liaison between Principal Investigators and the Institutional Review Board (IRB) and the Office of Sponsored Programs (OSP). Tracks all submissions to IRB and OSP, and maintains timely turnaround of all documents to avoid delays in study initiation and/or progress.
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Work closely with collaboratorsMaintain/Assist project documentation including IRB and prepare knowledge transfer materials. Preferred QualificationsThe ideal candidate holds a or degree in mechatronics, electrical computer engineering, biomechanics, or a related academic field, with specific experience in one or more of the following areas:- Programming in Python, Matlab, Simulink Real-time or similar- Mechatronics system development and real-time control- Experience in Arduino, Raspberry pi or similar- Wearable Sensors (IMUs, EMG, ECG, Foot pressure sensor, etc.
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Knowledge of medical/oncology process and terminology; experience and knowledge of Institutional Review Board (IRB) policy and procedure; background in science/medicine preferably in hematology/oncology.
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As a research administrator with broad-ranging responsibilities, the Director oversees three faculty who manage the Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and student research programs on a part-time basis.
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Understanding of IRB, and/or IACUC (Institutional Animal Care and Use Committee) research protocols and process. Coordinate administrative, IRB, and/or IACUC (Institutional Animal Care and Use Committee) approval of proposed research protocols.
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Extensive working knowledge of FAR, Cost Accounting Standards, Office of Management and Budget circulars, sponsored guidelines, clinical research regulatory environment, including FDA, regulations, IRB review and approval process and Good Clinical Practice (GCP.
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The Educator and Trainer ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). In collaboration with the Associate Dean for Cancer Clinical Research and the Administrative Director of the Cancer Institute Clinical Trials Office, the Workforce Development Educator and Trainer supports the growth and development of the Penn State Clinical Trials Office (CTO) by achieving strategic objectives including overseeing multiple project activities related to training and education of clinical research staff and investigators.
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ERA of non-sponsored agreements through the UT Research Management Suite: Agreements Module and eProtocol (Material Transfer Agreements (MTA), Non-Disclosure Agreements (NDA), Data Use Agreements (DUA), Memoranda of Understanding (MOU), Technology Control Plan (TCP), Confidential Data Control Plans (CDCP), IRB (for human subject protocols), and IACUC (for animal research protocols.
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Maintain a list of all studies closed w/ the IRB and docs sent to Iron Mtn. They will work with PIs, clinical coordinators and the IRB to make sure regulatory documents are approved and correct for all of the pharmaceutical research studies in medical oncology.
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