• Institutional Review Board

    Morehouse School Of Medicine (Atlanta, GA)
    …research proposals and amendments applications according to institutional and Institutional Review Board ( IRB ) policies and procedures and federal ... Institutional Review Board Analyst...the applicable regulations and policies, on how to prepare quality IRB submissions, including the preparation of… more
    Morehouse School Of Medicine (10/15/24)
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  • Clinical Research Coordinator Associate

    University of Michigan (Ann Arbor, MI)
    …to work with minimal supervision with diverse teams of physicians, coordinators, collaborators, Institutional Review Board , and Office of Research and ... Clinical Research Coordinator Associate underfill Clinical Research Coordinator Technician, Clinical Research...space in person + Design work flow and develop quality assurance processes for study start up,… more
    University of Michigan (11/04/24)
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  • Clinical Research Coordinator Intermediate

    University of Michigan (Ann Arbor, MI)
    …Assist with writing, editing, and renewing Institutional Review Board applications; maintain version trackers for IRB applications, informed consent ... experience and mastery of all job duties from the CRC- Associate position on the Michigan Medicine CRC Career Ladder...clinical research activities across the competency domains and conducts quality assurance / quality control checks on… more
    University of Michigan (11/04/24)
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  • Associate Director, Research Planning…

    MD Anderson Cancer Center (Houston, TX)
    …knowledge of the research process in compliance with institutional policies, Institutional Review Board and federal regulations. * Develop metrics to ... is to provide strategic planning and administrative oversight of large-scale multi- institutional clinical and translational research activities. The Associate more
    MD Anderson Cancer Center (10/30/24)
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  • Clinical Research Coordinator

    Hackensack Meridian Health (Paramus, NJ)
    …documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. ... to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries...shipment of specimens. + Prepares for or participate in quality assurance audits conducted by study sponsors,… more
    Hackensack Meridian Health (10/22/24)
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  • Clinical Research Coordinator III

    University of Florida (Lake County, FL)
    …preparation of a protocol ie informed consent, telephone script + Performs quality assurance ensuring proper maintenance of regulatory binder, protected health ... research participant recruitment, including human-subject protection, health studies and Institutional Review Boards SKILLS + Clinical-trials management systems… more
    University of Florida (10/05/24)
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  • OPS Clinical Research Coordinator

    University of Florida (Lake County, FL)
    …preparation of a protocol ie informed consent, telephone script + Performs quality assurance ensuring proper maintenance of regulatory binder, protected health ... research participant recruitment, including human-subject protection, health studies and Institutional Review Boards SKILLS Clinical-trials management systems… more
    University of Florida (10/05/24)
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  • Associate Academic Research Scientist…

    Emory Healthcare/Emory University (Atlanta, GA)
    …Aids in writing IACUC, IRB , Biosafety and other approval documents. + Oversees quality assurance of research conducted by other team members. + May assist in ... of Hematology and Oncology within Emory's School of Medicine is seeking an Associate Scientist with significant experience in immunology, working with in vitro and… more
    Emory Healthcare/Emory University (10/16/24)
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  • Clinical Research Coordinator - Genitourinary…

    Dana-Farber Cancer Institute (Boston, MA)
    …for protocol eligibility, obtain informed consent, and register study participants with the Quality Assurance Office for Clinical Trials (QACT). Some travel may ... entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB ...start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site… more
    Dana-Farber Cancer Institute (10/12/24)
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  • Grant And Contract Manager

    University of Washington (Seattle, WA)
    …supervisor and department contacts. Quality Assurance (10%): * Conduct a quality control review of all proposals to ensure each application is meeting ... requirements and department and school policies before being routed in SAGE for campus review . * Analyze the quality assurance results to identify… more
    University of Washington (09/04/24)
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  • GU Research Program Manager (Cancer Center)

    University of Pennsylvania (Philadelphia, PA)
    …closely with major internal (PI, CRU Central - Operations, Regulatory, Education/ QA , Budget, Legal, Finance, Billing Compliance , Infusion/CHPS, Investigational ... Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate...source document tools, show vigilance in patient safety, protocol compliance and data quality . Adhere to the… more
    University of Pennsylvania (10/27/24)
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  • Assoc Dean for Research - Professor

    University of Miami (Coral Gables, FL)
    …to support the school, programs, and students. + Oversee research compliance , including IRB and quality assurance procedures. + Represent the Dean and ... faculty or staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . Associate more
    University of Miami (10/06/24)
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  • Clinical Research Nurse 2

    Rush University Medical Center (Chicago, IL)
    …research study. 25. Develops, implements, and communicates process and procedures for data quality assurance and safety monitoring. 26. Accountable to PI for ... exemplary patient care while ensuring the protocol is conducted in a high- quality manner. Educates clinical staff and physicians regarding study. Updates clinical… more
    Rush University Medical Center (09/07/24)
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  • Clinical Research Coordinator

    Providence (Portland, OR)
    …by working collaboratively with sponsors, monitors, investigators, regulatory/contract CRA, and IRB to establish research plans and project timetables and coordinate ... to study sponsor. 3) Assist with the implementation of QA tools and the conduct of QA ...to ensure the adherence of study protocol and the compliance of clinical trials to applicable regulations; assist with… more
    Providence (10/14/24)
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