• IRB Specialist II Research…

    AdventHealth (Orlando, FL)
    …accuracy and consistency. The IRB Specialist II provides training for IRB Office Coordinators, external IRB review processes, and the IRB ... 500, Orlando, FL 32803 **The role you'll contribute:** The IRB Specialist II is knowledgeable...preferably in an academic or medical setting. + Certified Institutional Review Board Professional This… more
    AdventHealth (07/27/24)
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  • Live Support, Clinical Research Operations…

    Stanford University (Stanford, CA)
    …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Live Support, Clinical Research Operations Specialist II (REACT) (Fixed-Term: 12 months)...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
    Stanford University (07/10/24)
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  • Research Grant Specialist II

    Cedars-Sinai (Los Angeles, CA)
    …local agency requirements, including, the Food and Drug Administration (FDA) and local Institutional Review Board . This position is hybrid **Primary Duties ... superb clinical care and superior outcomes. The Research Grant Specialist II works with Principal Investigator to...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
    Cedars-Sinai (08/24/24)
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  • Clinical Research Data Specialist II

    Cedars-Sinai (Los Angeles, CA)
    …and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Duties and Responsibilities** + May ... nationally for excellence in research!** The Clinical Research Data Specialist II manages the data for assigned...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
    Cedars-Sinai (08/02/24)
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  • IRB Specialist II

    Actalent (Orlando, FL)
    …work on site every other week on Wednesday/Thursday Location: Orlando, Florida Position Overview As an IRB Specialist II , you will be an expert in state and ... will train IRB Office Coordinators, manage external IRB review processes, and oversee the ...in an academic or medical setting. Certification: + Certified Institutional Review Board Professional (CIP).… more
    Actalent (09/19/24)
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  • Research Specialist II

    University of Rochester (Rochester, NY)
    …other tissues. With latitude for modifying methods and techniques, records, the specialist will compute and analyze test data; prepare reports and make ... recommendations. Specifically, the research specialist will perform experiments involving cell purification, storage, culture, flow cytometry, RNA or DNA extraction,… more
    University of Rochester (08/23/24)
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  • Public Health Project Spec II

    University of Rochester (Rochester, NY)
    …at The University of Rochester is seeking a full-time Public Health Project Specialist II to coordinate the development and implementation of a federally ... progress reports to the funding agency when necessary. + Develops and maintains IRB documentation (such as recruitment materials and data use agreements) as well as… more
    University of Rochester (07/26/24)
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  • Clinical Trials Regulatory Specialist I

    Emory Healthcare/Emory University (Atlanta, GA)
    …and monitors practices to ensure regulatory documentation involving clinical trials complies with Institutional Review Board ( IRB ) policies and ... trial portfolio. KEY RESPONSIBILITIES: + Assists regulatory team (Regulatory Specialist II and III) in research efforts...to various review committees, including internal scientific review boards, the IRB and sponsoring entities.… more
    Emory Healthcare/Emory University (07/31/24)
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  • Human Subject Res Coord II

    University of Rochester (Rochester, NY)
    …at The University of Rochester is seeking a full-time Human Subject Research Specialist , Level II , to coordinate human subject research activities. The division ... data management, interactions with subjects and communication with regulators (eg CRO, IRB ). The coordinator will also provide cross-coverage of other trials in the… more
    University of Rochester (08/06/24)
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  • Human Sub Research Spec II

    University of Rochester (Rochester, NY)
    …University of Rochester is seeking a part-time (20 hours/week) Human Subject Research Specialist , Level II , to coordinate human subject research activities. The ... recruitment strategies, information, data systems and study management systems; development, review and approval of case report forms (CRFs) and study-specific… more
    University of Rochester (06/30/24)
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  • Clinical Research Coordinator

    Actalent (Rochester, NY)
    …at The University of Rochester is seeking a full-time Human Subject Research Specialist , Level II , to coordinate human subject research activities. The division ... data management, interactions with subjects and communication with regulators (eg CRO, IRB ). The coordinator will also provide cross-coverage of other trials in the… more
    Actalent (09/17/24)
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  • Research Specialist | The Versace Lab

    UPMC (Pittsburgh, PA)
    …on investigating i) the effects of adolescent concussion on the developing brain, ii ) the extent to which these interfere with changes in pubertal hormones in ... data is saved, backed-up, and preprocessed in a timely manner; assisting with IRB - and NDA-related activities; as well as other duties related to the documentation… more
    UPMC (09/18/24)
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  • Clinical Trials Research Coverage Analyst

    Rush University Medical Center (Chicago, IL)
    …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents in order to prepare a ... and services required in a clinical research project. * Review clinical research protocols and determine which procedures are...trial under CMS Clinical Trial policy. * Coordinate with IRB staff and the investigator if the IRB more
    Rush University Medical Center (08/30/24)
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  • Clinical Trials Research Coverage Analyst…

    Rush University Medical Center (Chicago, IL)
    …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents to prepare a billing plan ... and services required in a clinical research project. * Review clinical research protocols and determine which procedures are...trial under CMS Clinical Trial policy. * Coordinate with IRB staff and the investigator if the IRB more
    Rush University Medical Center (07/25/24)
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  • Clinical Assistant Professor Of Applied Behavior…

    University of Michigan (Dearborn, MI)
    …### or [email protected] , Academic Program Manager, ABA Clinical Faculty Search. Review of applications will begin in early Fall 2024 and will continue until ... (25-40%) + Fulfill the position of Instructor of Record for ABA II Practicum, Behavioral Assessment Practicum, Research Methods in ABA Practicum (includes regular… more
    University of Michigan (09/03/24)
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  • Director Medical Staff Services

    BayCare Health System (Clearwater, FL)
    …medical staff credentials committees, central Continuing Medical Education (CME), and Institutional Research Board ( IRB ). **Minimum Qualifications:** ... Health System operates 16 hospitals, including a children's hospital with a level II pediatric trauma center; has a robust physician group, BayCare Medical Group… more
    BayCare Health System (09/19/24)
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  • Manager, Clinical Trials & Charge Capture - 100%…

    Rush University Medical Center (Chicago, IL)
    …from the vendors are received and accurate based upon agreed costs. * Review accuracy of the Clinical Research Coverage Analyst and Clinical Research Financial ... Analyst daily work. * Review / audit of daily activity of the Clinical Research...Cycle colleagues, study teams, patients, Office of Research Affairs, IRB , RUMC Compliance, and all partners in the Research… more
    Rush University Medical Center (09/05/24)
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