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St. Jude is a highly interactive environment offering its faculty a remarkable opportunity to perform cutting-edge independent and collaborative research while receiving long-term institutional support past start-up to facilitate innovation and discovery.
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This position will manage activities pertaining to the Protocol Review and Monitoring Committee (PRMC) which primary goal is to ensure that institutional, industry-sponsors, and externally peer reviewed cancer research studies involving human subject conducted under the auspices of the SCCC are (1) scientifically and statistically sound; (2) appropriately designed; (3) feasible for completion; and (4) if applicable, in compliance with NIH guidelines for clinical trials.
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IRB: UCLA’s Institutional Review Board (Application to Involve Human Subjects in Research form, study-specific Informed Consent Form, HIPAA Authorization, subject recruitment documentation and requests) c.
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In partnership with the Office of Research Affairs and Research Compliance ensures Standard Operating Procedures (SOPs) are implemented and documented in accordance with study sponsor, Principal Investigator, and regulatory agency specifications.
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Posted Job TitleClinical Research Coordinator B/C (Pharmacology)Job Profile TitleClinical Research Coordinator BJob Description SummaryWe are looking for a full-time experienced clinical research coordinator (CRC - level B or C) to work in a fast-paced translational immunology research laboratory.
$42,953 - $65,861 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The incumbent has a diverse range of responsibilities, which includes the following: Support the Head of the IDR with developing and coordinating nonhuman primate (NHP) infectious disease study plans; formulating budgets for NHP studies; and preparing and maintaining Institutional Animal Care and Use and Institutional Biosafety protocols for NHP studies.
$58,939 - $112,519Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH.
$61,242 - $86,121 a yearExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The Department is comprised of six major areas of undergraduate study: Art History, Ceramics, Graphic Design and Digital Media, Painting/Drawing/Printmaking, Photography, and Sculpture. General Description / Primary Purpose The University of North Florida’s Department of Art and Design invites applications for a tenure-track Assistant Professor in Painting and Drawing beginning in Fall 2024The University of North Florida’s Department of Art and Design is an accredited institutional member of the National Association of Schools of Art and Design (NASAD.
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WPI is committed to creating an inclusive workplace where everyone feels valued and respected; a place where every student, faculty and staff member can be themselves, so that they can study, live, and work comfortably, to reach their full potential, and make meaningful contributions in order to meet departmental and institutional goals.
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The Penn State College of Medicine, Department of Psychiatry and Behavioral Health, in Hershey, PA, is seeking a Human Research Technologist to organize lab materials, conduct data collection, interact with study participants, monitor incoming data for accuracy, ensure lab compliance and safety, and maintain study information/databases.
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Assures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.
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May collaborate with Research Site Leader in the study selection process. Responsible for preparing study-related documentation such as protocol worksheets, adverse event reports, institutional review board documents, and annual continuing review reports.
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Monitors the occurrence of clinical adverse events, reporting any to the PI, the study sponsor and Institutional Review Board (IRB). Responsible for assisting with IRB requirements for each study including meeting institutional educational requirements, submitting documents for review, adverse event reporting and annual reviews.
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Document and collect data and/or samples for research related procedures performed during participant study visits. Maintain strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines.
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Performs real-time data review of Animal Rule/GLP study data in both hard copy and electronic format and generates and maintains study notebooks according to institutional guidelines (15.
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