• Sr . Specialist , RA

    West Pharmaceutical Services (Exton, PA)
    Sr . Specialist , RA Project Management Requisition ID: 66487 Date: Sep 12, 2024 Location: Exton, Pennsylvania, US Department: Regulatory Affairs ... and planet through our sustainability efforts. **Job Summary:** This Senior Specialist , Regulatory Project...execution of project objectives in line with regulatory affairs ( RA ) team's priorities.… more
    West Pharmaceutical Services (09/11/24)
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  • Senior Regulatory Affairs

    Bausch + Lomb (Trenton, NJ)
    …cycle to interdisciplinary project teams and to appropriate management level in Regulatory Affairs , R&D, TechOps and Supply Chain as appropriate in a timely ... company functions during Regulatory Authority inspections. + Serve as Regulatory Affairs representative on facility/site Local Change Management Boards. +… more
    Bausch + Lomb (09/04/24)
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  • Clinical Research Monitoring Specialist

    University of Pennsylvania (Philadelphia, PA)
    …and resources, and much more. Posted Job Title Clinical Research Monitoring Specialist Senior (Cancer Center) Job Profile Title Clinical Research Monitoring ... Specialist Senior Job Description Summary The Abramson...IND/IDE in both adult and pediatric research. Must understand regulatory affairs and their applications to Quality… more
    University of Pennsylvania (07/04/24)
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  • Senior Specialist , Lead Database…

    Merck (West Point, PA)
    …new processes and technologies. + Broad knowledge of Clinical Development and Regulatory Affairs requirements. + The ability to multi-task, work independently, ... technical initiatives. + Supporting the clinical database manager/supervisor in project planning, manpower projections, and resource allocation across therapy areas… more
    Merck (09/06/24)
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  • Clinical Research Quality Specialist C…

    University of Pennsylvania (Philadelphia, PA)
    …regulations, GCP and IND/IDE in both adult and pediatric research. Must understand regulatory affairs and their applications to Quality Control and Quality ... Monitoring (DOCM) is seeking a The Clinical Research Quality Specialist , Sr . to support our clinical research...centers. Additional experience in clinical research ie Data Management, Project Management, Drug Safety are a strong plus. The… more
    University of Pennsylvania (08/03/24)
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