• Institutional Review Board

    Geisinger (Danville, PA)
    …and materials, as well as IRB meeting minutes. + Records convened Institutional Review Board discussion and stipulations, and ensures accurate ... for regulatory and compliance issues. Provides technical support for Institutional Review Board system users...Administers educational programs pertaining to human research protections and IRB review processes for IRB more
    Geisinger (06/25/25)
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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 ... monitoring and submitting AEs, SAEs, and UADEs reports to the Investigator and Institutional Review Board ( IRB ) per protocol, federal, and … more
    University of Pennsylvania (06/18/25)
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  • Clinical Research Nurse

    Actalent (Philadelphia, PA)
    …documents, informed consents, case report forms, and source documents. The preparation of Institutional Review Board ( IRB ) applications will also ... documents, informed consents, case report forms, and source documents. + Prepare Institutional Review Board ( IRB ) applications. Essential Skills +… more
    Actalent (08/19/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …of multiple clinical research projects investigating surgical outcomes in the US Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... clinical research projects investigating surgical outcomes in the US Assist with Institutional Review Board ( IRB ) filings and inquiries, and assist… more
    University of Pennsylvania (06/10/25)
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  • Clinical Research Coordinator B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …duties and responsibilities as assigned Regulatory Responsibilities: + Prepare and process all Institutional Review Board ( IRB ) documentation through the ... Initiation meetings + Obtain slides from pathology and ship to sponsor/independent review per protocol guidelines. + Obtain records required to complete case report… more
    University of Pennsylvania (06/16/25)
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  • Clinical Research Coordinator B (Department…

    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 ... institutional or study related committees and personnel (eg, IRB , DSMC, DSMB/Medical Monitor) according to applicable regulations and...to all applicable PENN institutional committees for review and approval to start trial (eg, IRB more
    University of Pennsylvania (05/26/25)
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  • Clinical Research Coordinator A (Department…

    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 ... team members in retrieval and provision of documentation required for IRB submission/renewals in accordance with guidelines; continuing review , modification,… more
    University of Pennsylvania (08/09/25)
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  • Clinical Research Coordinator A (Abramson Cancer…

    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 ... + Adhere to all University of Pennsylvania, informed consent form (ICF), and IRB guidelines. Position is contingent upon funding. QUALIFICATIONS: BA/BS and 1-2 year… more
    University of Pennsylvania (07/20/25)
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  • Clinical Research Coordinator B (Surgery Research…

    University of Pennsylvania (Philadelphia, PA)
    …sites and assists in the management of multisite trials. Job Description Prepare and process all Institutional Review Board ( IRB )through the IRB and ... other regulatory groups as appropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events . Coordinate, organize and maintain all documentation required by sponsor or CRO (case report forms, source… more
    University of Pennsylvania (06/03/25)
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  • Clinical Research Coordinator B/C (Palliative…

    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 ... or other programs. + Preparing study reports, annual reviews, and Institutional Review Board documentation + Liaising with key stakeholders, including… more
    University of Pennsylvania (08/20/25)
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