• Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Addresses adverse events per protocol, advocating for study more
    University of Miami (12/20/25)
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  • Research Support Specialist (N)

    University of Miami (Miami, FL)
    …procedures according to the protocol.3. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants.7. Addresses adverse events per protocol, advocating for study more
    University of Miami (12/20/25)
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  • Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... to work onsite on the UHealth campus. The CROWN Study 's Clinical Research Coordinator 1 to oversee study...supervisor of adverse events, including those reported by study participants. + Addresses adverse events per protocol, advocating… more
    University of Miami (12/20/25)
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  • Clinical Research Coordinator 1 - Crane Lab

    University of Miami (Miami, FL)
    …procedures according to the protocol.2. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants.6. Addresses adverse events per protocol, advocating for study more
    University of Miami (12/20/25)
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  • Professional Engineer - Public Works

    City of Lakeland (Lakeland, FL)
    …and engineers. Work includes the preparation, review, and acceptance of studies , reports, designs, plans, specifications, and cost estimates for the project. ... is required. Work is performed under the general supervision of an administrative supervisor and is evaluated upon completion. The direction will be exercised over… more
    City of Lakeland (11/27/25)
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  • Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Addresses adverse events per protocol, advocating for study more
    University of Miami (12/20/25)
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  • Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …procedures according to the protocol.2. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants.6. Addresses adverse events per protocol, advocating for study more
    University of Miami (01/09/26)
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  • Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …procedures according to the protocol. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. Addresses adverse events per protocol, advocating for study more
    University of Miami (01/06/26)
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  • Clinical Research Coordinator 1 (A)

    University of Miami (Miami, FL)
    …procedures according to the protocol. + Coordinate routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Address adverse events per protocol, advocating for study more
    University of Miami (12/20/25)
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  • Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Addresses adverse events per protocol, advocating for study more
    University of Miami (12/20/25)
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