• Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB more
    University of Pennsylvania (10/03/25)
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  • Clinical Research Coordinator 3 (A)

    University of Miami (Miami, FL)
    …a proven experience in managing regulatory documentation and submissions to entities such as the Institutional Review Board ( IRB ) and the Food and Drug ... OBGYN has an exciting opportunity for a full-time Clinical Research Coordinator 3 to work in Miami,...initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB more
    University of Miami (08/23/25)
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  • Research Coordinator

    Stanford University (Stanford, CA)
    …strategies for recruitment, data quality control procedures and processes). May follow up with Institutional Review Board ( IRB ) to ensure renewals are ... and communications within appropriate systems, conduct qualitative interviews, and review survey answers. The Research Coordinator...control procedures and processes). May follow up with the Institutional Review Board ( IRB more
    Stanford University (10/07/25)
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  • Research Coordinator - Dr. Golden's…

    University of Washington (Seattle, WA)
    …procedures, recruitment, monitoring study progress, data analysis, and work with the UW institutional review board . Current projects include an NIH-funded ... Diseases_** **has an outstanding opportunity open for a** **_Temporary_** ** Research Coordinator .** The Research ...* Research specific training in Protection of Human Research Subjects. * Self-starter and able… more
    University of Washington (08/20/25)
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  • Clinical Research Coordinator A

    University of Pennsylvania (Philadelphia, PA)
    …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical...of a team, as well as independently; knowledge of IRB and human research protection… more
    University of Pennsylvania (07/24/25)
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  • Clinical Research Coordinator II

    Loyola University Chicago (Chicago, IL)
    …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. * Assemble ... Clinical Research Coordinator II Thank you for...complete study documents/case report forms. * Ensure compliance with research protocols, and review and audit case… more
    Loyola University Chicago (10/02/25)
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  • Research Coordinator I - Dermatology

    Dartmouth Health (Lebanon, NH)
    …standards operating procedures for the execution of clinical trial operations, including timely Institutional Review Board ( IRB ) submissions meeting ... Overview Clinical Research Coordinator I works closely with...with regulatory processes. * Maintains basic current understanding of IRB and Dartmouth-Hitchcock Health (D-HH) Institutional processes.… more
    Dartmouth Health (09/18/25)
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  • Clinical Research Coordinator

    Dialysis Clinic, Inc. (Albany, GA)
    …and post-study closure. They prepare documentation for submission for review by the Institutional Review Board ( IRB ), recruit and screen study ... including the collection, preparation, maintenance, and submission of numerous study documents: Institutional Review Board ( IRB ) applications, CV's,… more
    Dialysis Clinic, Inc. (09/19/25)
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  • Manager, Clinical Research

    University of Rochester (Rochester, NY)
    …of experience or + Equivalent combination of education and experience + Experience as Human Subject Research Coordinator 1 preferred **KNOWLEDGE, SKILLS AND ... state, sponsor and/or institutional regulations, policies and practices related to human subject research . Will be both enrolling patients and participating… more
    University of Rochester (10/10/25)
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  • Clinical Research Coordinator 2…

    Stanford University (Stanford, CA)
    … Subjects Panel. + Coordinate new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Complete annual reports ... Clinical Research Coordinator 2 - Surgical Planning **School of...to Institutional Review Board , CSTA, FDA and other regulatory agencies. Submit… more
    Stanford University (10/07/25)
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