• Director Therapy Area Head, Statistical…

    Teva Pharmaceuticals (West Chester, PA)
    …implement programming strategies that enable high-quality, efficient, and compliant outputs for regulatory submissions and clinical trial reporting. + Lead and ... and vendors + Partner with cross-functional stakeholders (Statistics, Data Management, Clinical Development, Regulatory ) to ensure alignment and successful… more
    Teva Pharmaceuticals (09/05/25)
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  • Research Associate - College of Engineering…

    Carnegie Mellon University (Pittsburgh, PA)
    …+ Manages laboratory operations, including supply procurement, equipment maintenance, and regulatory compliance . + Contributes to writing and reviewing technical ... in the project. You will evaluate product-market fit, identify potential regulatory and translational pathways, and support strategies for moving lab innovations… more
    Carnegie Mellon University (09/06/25)
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  • CRA II / Sr. CRA

    ICON Clinical Research (Blue Bell, PA)
    …Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. + Conducting ... trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. **What You Will Be...Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. +… more
    ICON Clinical Research (09/06/25)
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  • Senior Medical Science Liaison

    Cardinal Health (Harrisburg, PA)
    …three hours. We also provide customers the support they need in regulatory compliance , reimbursement, continuing education, information management and other ... in applicable field highly preferred + Current working knowledge of US legal, regulatory , and compliance regulations & guidelines to industry interactions with… more
    Cardinal Health (09/05/25)
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  • Cardiac Surgery Program Manager (Department…

    University of Pennsylvania (Philadelphia, PA)
    …both sites; continually assessing staff performance at all phases of orientation, assess clinical staff compliance with protocol on ongoing basis to minimize ... issues of non- compliance at both sites. Provide resources and mentorship for...and informed consents documents in collaboration with faculty. + Regulatory -Financial-Training/Continuing Education: Negotiate clinical trial agreements and… more
    University of Pennsylvania (08/03/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
    Merck (07/26/25)
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  • Director, Prospective + Concurrent Risk Adjustment…

    Datavant (Harrisburg, PA)
    …care management platforms, and third party integrations. + Balance innovation with compliance , audit defensibility, and clinical integrity across all product ... managers and product designers and collaborate deeply with data science, clinical experts, engineering, and commercial teams to accelerate innovative solutions that… more
    Datavant (08/08/25)
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  • Medical Assistant

    Penn Medicine (Berwyn, PA)
    …outdated items. Performs daily code/crash cart checks as assigned. + Other / Regulatory + Ensures compliance with all applicable federal, state, and local ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
    Penn Medicine (09/04/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects. + Develop and execute statistical analysis… more
    Merck (09/03/25)
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  • Sr. Scientist, Statistical Programmer, Late Stage…

    Merck (North Wales, PA)
    …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
    Merck (09/05/25)
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