• Clinical Research Coordinator -Part time

    Dayton Children's Hospital (Dayton, OH)
    …Department Specific Job Details: Required: Associates Degree 1-2 years of Research Assistant , Research Coordinator , or Regulatory Coordinator experience ... Children's - Main CampusDepartment:Surgery AdministrationSchedule:Part timeHours:20Job Details:The Clinical Research Coordinator will perform clinical research activities under the general… more
    Dayton Children's Hospital (07/22/25)
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  • Clinical Research Coordinator

    Actalent (Tacoma, WA)
    …will have taken full responsibility in previous roles, not merely as a research assistant or backup coordinator . This role involves frequent use of EPIC and ... Oncology Clinical Research Coordinator Job Description We are seeking a dedicated...in cardiology and oncology. + Handle regulatory tasks, including IRB submissions. + Engage in sponsor correspondence, excluding budget… more
    Actalent (08/19/25)
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  • Administrator - Institutional Review

    HonorHealth (AZ)
    …Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... accordance with (45 CFR 46.101-409) the IRB Coordinator facilitates initial and continuing review of...This includes initial determinations regarding expedited, exempt, or full board review , as well as human subject… more
    HonorHealth (07/30/25)
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  • Clinical Research Coordinator 2…

    Georgetown Univerisity (Washington, DC)
    …with an Associate's Degree and 5 years' minimum work experience as a Clinical Trial Coordinator or Clinical Research Assistant + In addition to a BA/BS or AA ... experience + 3 year minimum experience will be as a Clinical Trial Coordinator , Clinical Research Assistant , or equivalent position; However, as this is… more
    Georgetown Univerisity (07/18/25)
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  • PS Clinical Research Coord

    University of Utah (Salt Lake City, UT)
    …role will have significant responsibility for preparing, submitting, and maintaining institutional review board ( IRB ) protocols in coordination with ... 20. May perform functions required of the Clinical Research Assistant or Clinical Research Coordinator as necessary....experience in human subjects research, particularly institutional review board ( IRB )… more
    University of Utah (08/20/25)
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  • Clinical Research Coordinator I, Laboratory…

    Cedars-Sinai (Los Angeles, CA)
    …staff meetings. + Works closely with investigators and regulatory staff or directly with Institutional Review Board ( IRB ) to submit adverse events, ... Diploma preferred. + 1 year of experience as a clinical research coordinator or clinical research associate/ assistant preferred. + Demonstrated ability to… more
    Cedars-Sinai (06/07/25)
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  • Program Coordinator , Healthy Libraries…

    Stony Brook University (Stony Brook, NY)
    …The Program in Public Health at Stony Brook University (SBU PPH) seeks a staff assistant for the position of Program Coordinator for the Stony Brook Medicine ... Program Coordinator , Healthy Libraries Program **Required Qualifications (as evidenced...Writing:** * Assist HeLP leadership to prepare and submit IRB protocols to ensure use of de-identified human subject… more
    Stony Brook University (08/21/25)
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  • Research Coordinator TRI Cardio Cheektowaga

    Catholic Health (Buffalo, NY)
    …may be credentialed as a Registered Professional Nurse (RN), Certified Research Coordinator (CRC), or Certified Medical Assistant + Candidates should also ... Schedule: Days Hours: 8:30am -4:30pm M-F Summary: The Research Coordinator is a healthcare position that will involve the...+ Knowledge of FDA rules and regulations, GCP, and IRB processes and procedures + Strong interpersonal and organizational… more
    Catholic Health (07/09/25)
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  • Clinical Research Coordinator B/C…

    University of Pennsylvania (Philadelphia, PA)
    …maintain all regulatory clinical trial documents and protocols ensuring compliance with the Institutional Review Board , the Abramson Cancer Center Trial ... Data Capture) or other programs. + Preparing study reports, annual reviews, and Institutional Review Board documentation + Liaising with key stakeholders,… more
    University of Pennsylvania (08/20/25)
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  • Clinical Research Coordinator II Tri…

    AdventHealth (Orlando, FL)
    …and adherence to research protocols._ _Serves as liaison between Principal Investigators and the Institutional Review Board ( IRB ) and the Office of ... **Clinical Research Coordinator II AdventHealth Orlando** **All the benefits and...research and administration._ _Reviews all elements of the current institutional IRB approved informed consent (IC) document,… more
    AdventHealth (08/23/25)
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