• Research Nurse Coordinator II (Hybrid),…

    Cedars-Sinai (Beverly Hills, CA)
    …which are variable to accommodate patient visits, investigator schedules, study needs, meetings, staff coverage, audits/monitoring visits or otherwise assigned ... research visits, assisting with research billing inquiries, and ensuring flow sheets and study requirements are accurately followed. As part of the larger Phase I… more
    Cedars-Sinai (11/15/25)
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  • Clinical Research Nurse C/D (Abramson Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …Research Unit seeks a full-time, Clinical Research Nurse (CRN) to conduct studies involving a wide variety of investigational products and various sponsors. This ... collaboration with Research Team Leaders and Principal Investigators with initiating study procedures for new IITs and industry-sponsored clinical trials. Manage all… more
    University of Pennsylvania (11/14/25)
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  • Clinical Research Associate 3

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Ensures coordination of an accelerated study start-up ... trials to ensure timelines and metrics are met and maintained throughout the study . **Primary responsibilities include:** + Tracking study specific tasks and… more
    Grifols Shared Services North America, Inc (11/08/25)
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  • Epi Research Coordinator 1 - Temporary, Full Time

    Rush University Medical Center (Chicago, IL)
    study protocols. **Responsibilities:** * Coordinates aspects of less complex research studies including, but not limited to, study start-up, initiation ... coordinates Epidemiological, Behavioral or Human Translational, or Population Health research studies and performs a variety of duties including the collection… more
    Rush University Medical Center (11/08/25)
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  • Clinical Drug Supply Manager

    ICON Clinical Research (Blue Bell, PA)
    …IOPS requirements; Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical development plan; Works with ... to determine resourcing needs; Provides input to the development of IP-related study documents including protocols, study and pharmacy manuals; Responsible for… more
    ICON Clinical Research (11/05/25)
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  • Medical Affairs Clinical Specialist - JJMT…

    J&J Family of Companies (Irvine, CA)
    …& Johnson's clinical development strategy. **Key Responsibilities:** + Serve as the primary study medical lead for company sponsored clinical studies . + Support ... the current medical literature. + Contribute to drafting and reviewing of study reports for assigned studies to include annual reports (APR), study close out… more
    J&J Family of Companies (01/10/26)
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  • Site Manager, Onsite

    IQVIA (Lilburn, GA)
    …strong interpersonal and team building skills. The employee, working closely with study team members, will achieve study objectives and corporate goals. ... + Works closely with Business Development and Feasibility on study placement + Accountable for enrollment success at sites...+ Accountable for enrollment success at sites across all studies ; works to understand revenue expectations + Develops and… more
    IQVIA (01/09/26)
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  • Data Science Program Lead III

    AbbVie (North Chicago, IL)
    …program- and study -level strategies. Supports governance of assigned programs and studies , both within and outside DSS. Assigned programs may include programs of ... role is a key to ensuring successful delivery against the program- and study -level accountabilities assigned to Data and Statistical Sciences. * This role requires… more
    AbbVie (01/07/26)
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  • Student Programs Advisor II

    University of Southern California (Los Angeles, CA)
    …Student Programs Advisor II ( Study Abroad Advisor) in the Office of Overseas Studies . The largest and oldest of the USC schools, USC Dornsife functions as the ... the humanities, social sciences and natural sciences. The Office of Overseas Studies also serves undergraduates from the other schools at USC. Responsibilities… more
    University of Southern California (01/07/26)
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  • SR Scientist, Clinical

    Boehringer Ingelheim (St. Joseph, MO)
    …extensions and maintaining existing licensed products. This role provides clinical study design and implementation including resource and budget planning from ... protocol to execution and to final study report for submission to regulatory agencies for animal...and reporting to achieve project milestones. + Designs clinical studies to earn label claims and new product licenses/marketing… more
    Boehringer Ingelheim (12/24/25)
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