• Research Specialist A (Department of Pathology…

    University of Pennsylvania (Philadelphia, PA)
    …Daily management of laboratory tools, documentations and processes to ensure regulatory compliance and timely completion of project/program deliverables, with close ... Daily management of laboratory tools, documentations and processes to ensure regulatory compliance and timely completion of project/program deliverables, with close… more
    University of Pennsylvania (11/14/25)
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  • Clinical Research Coordinator A

    University of Pennsylvania (Philadelphia, PA)
    …and their protection. + Assure compliance with the protocol and regulatory requirements includes: collecting, recording, and maintaining data and source ... documentation and maintaining regulatory binders through subject study completion. + Coordinate and...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
    University of Pennsylvania (11/14/25)
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  • Research Specialist A

    University of Pennsylvania (Philadelphia, PA)
    …collection, researching and writing animal protocols, preparing and submitting regulatory documentation, maintaining laboratory space, and ordering supplies. Job ... collection, researching and writing animal protocols, preparing and submitting regulatory documentation, maintaining laboratory space, and ordering supplies. Position… more
    University of Pennsylvania (11/14/25)
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  • Research Director C

    University of Pennsylvania (Philadelphia, PA)
    …translational and clinical research, and clinical trials. Additionally, they manage regulatory submissions (IRB, IACUC, RIS) and directly support research activities ... translational and clinical research, and clinical trials. Additionally, they manage regulatory submissions (IRB, IACUC, RIS) and directly support research activities… more
    University of Pennsylvania (11/06/25)
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  • Clinical Research Coordinator A/B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …multiple locations across the health system, biospecimen processing, and regulatory management. This position involves working directly with several Investigators ... of clinical trial databases using REDCap functionality. Maintain subject files and regulatory files per GCP. + Utilize Electronic Medical records to collect data… more
    University of Pennsylvania (11/02/25)
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  • Research Laboratory Technician C

    University of Pennsylvania (Philadelphia, PA)
    …management of laboratory tools, documentation and processes to ensure regulatory compliance and timely completion of project/program deliverables. Excellent ... and immunochemistry. + Collect data and documentation to ensure regulatory compliance. + Assist with inventory and ordering of...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
    University of Pennsylvania (10/21/25)
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  • Research Investigator Sr.

    University of Pennsylvania (Philadelphia, PA)
    …Conduct hands-on radiolabeling experiments in compliance with safety and regulatory standards. . Collaborate with interdisciplinary teams including synthetic ... Conduct hands-on radiolabeling experiments in compliance with safety and regulatory standards. . Collaborate with interdisciplinary teams including synthetic… more
    University of Pennsylvania (09/19/25)
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  • Research Specialist D

    University of Pennsylvania (Philadelphia, PA)
    …PET image analysis, PET drug manufacturing, therapeutic drug synthesis and related regulatory guidelines as a member of a small, multidisciplinary research group. ... PET image analysis, PET drug manufacturing, therapeutic drug synthesis and related regulatory guidelines as a member of a small, multidisciplinary research group.… more
    University of Pennsylvania (09/19/25)
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  • Clinical Research Coordinator C (Department…

    University of Pennsylvania (Philadelphia, PA)
    …Will problem-solve the challenges to implement a plan of action. Work with the regulatory manager to ensure that submissions to the IRB are completed in a timely ... I-IV clinical trials (10% Essential: 1),Prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
    University of Pennsylvania (09/10/25)
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  • Clinical Research Project Manager C

    University of Pennsylvania (Philadelphia, PA)
    …QC; study close out activities). + Develop, create and review regulatory submission and study documents/tools, including protocols, consents, annual reports, source ... writing assistance); and/or post award finance activities (invoicing, billing review). + Staff supervision: Assist and train direct and/or indirect research staff more
    University of Pennsylvania (11/11/25)
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