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Knowledge of regulatory requirements and ethical standards governing survey research in healthcare, including HIPAA and IRB guidelines. Advanced degree (e.g., PhD, MD, MPH) in public health, epidemiology, biostatistics, health services research, or a related field.
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Must complete NU's IRB CITI training before interacting with any participants & must re-certify every 3 years. Assists with IRB submissions and manages regulatory documents. The Northwestern campus sits on the traditional homelands of the people of the Council of Three Fires, the Ojibwe, Potawatomi, and Odawa as well as the Menominee, Miami and Ho-Chunk nations.
$49,850 - $70,419 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Identifies opportunities for process improvement; and implements and manages quality improvement initiatives to enhance office procedures, IRB performance, biosafety, and/or overall human subject’s protections.
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Compliance with the regulations requires administrative support of the chairperson of the Institutional Review Board for the Protection of Human Subjects ( IRB ). Certification from the Council for Certification of IRB Professionals ( CIP ) would be ideal.
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Reports adverse drug reactions and submits the appropriate documentation to the FDA, NCI and IRB. Provides assistance with IRB submissions. The Clinical Research Nurse Specialist manages post-transplant patients and contributes to multiple studies within the section of Transplant Surgery under supervision of the Principal Investigator (PI), Dr. Piotr Witkowski.
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Current Advanced Practice Nurse (APN) license in the State of Illinois or eligibility to receive by start date. Works with PI to coordinate hospital admissions, transplant procedures, and study related tests.
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Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well as. complete the necessary documents for IRB submission in a timely fashion. complete the necessary documents for IRB admission in a timely fashion.
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Regulatory compliance: Ensure that the research site is in compliance with applicable regulatory requirements, including institutional review board (IRB) approvals and FDA regulations. Regulatory compliance: Ensure that the research site is in compliance with applicable regulatory requirements, including institutional review board (IRB) approvals and FDA regulations.
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Proficiency in survey methodology, statistical analysis, and data visualization techniques, with expertise in software tools such as SPSS, SAS, R, or STATA. Innovation: Focus on the development and application of new methodologies, technologies, and techniques to gather data and insights including Machine learning AI, Mobile Optimized Surveys, Gamification, Behavioral economics, real-time feedback, Multimodal surveys, Blockchain technology, Virtual and Augmented reality.
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Ensuring the integrity and quality of clinical trials are maintained and conducted in accordance w/ federal, state, and local regulations, ICH/GCP guidelines, Institutional Review Board (IRB) approvals, and institutional policies and procedures.
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May need to work with principal investigator on IRB, ACUC, filing and compliance. Position Student Summer Researcher - RMC Medical Student Programs RMC. May need to work with principal investigator on IRB, ACUC, filing and compliance.
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The Research Associate I will assist the Principal Investigator with clinical trials management, IRB submissions, and conduct literature searches and writing for Ocular Graft Versus Host Disease research.
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Participates in developing and maintaining grant applications and supporting documentation for submission to the IRB and reports relevant research findings to IRB, Knowledge of anatomy and physiology and physical therapy treatments and modalities at a level normally acquired through completion of Doctoral degree from an accredited school of physical therapy.
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Completion and Submission of Clinical Trials Amendments: Ensure timely completion and accurate submission of all amendments to the Institutional Review Board (IRB), adhering to regulatory guidelines and protocols.
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The individual will assume the role of Privacy and HiPAA security officer and serve as a voting member of the IRB board. The individual will assume the role of Privacy and HiPAA security officer and serve as a voting member of the IRB board.
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irb job in Chicago, IL
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