• Senior Clinical Director Ambulatory

    Penn Medicine (Philadelphia, PA)
    …in this regard. Provides ongoing continuing education and skill validation of clinical staff. Quality, Patient Safety, and Regulatory Affairs: Partnership with ... alignment with Health System Requirements. In conjunction with the Vice-Chair of Regulatory Affairs, develop programs that enhance the clinical decision-making,… more
    Penn Medicine (08/07/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Harrisburg, PA)
    …global team members, other B&L departments (eg, R&D/Project Management, Clinical /Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, ... manage and monitor study related expenses to meet forecast. Regulatory Reports: + Provide Clinical Operations support in the timely coordination and execution of… more
    Bausch + Lomb (06/07/25)
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  • Oncology Early Stage Clinical Scientist…

    Pfizer (Collegeville, PA)
    …and external partners, such as project leaders, research units, biostatistics, regulatory affairs, clinical pharmacology, human genetics, translational oncology, ... Experience working with and solid understanding of related disciplines, eg, Clinical Operations, Safety, Biostatistics, Regulatory , Study Management, Pre-… more
    Pfizer (08/21/25)
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  • Clinical Research Coordinator B/C (Abramson…

    University of Pennsylvania (Philadelphia, PA)
    …needed. Coordinate non-therapeutic studies and complex Phase I, II, or III oncology clinical trials. + Assist the Regulatory Coordinator by preparing components ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Abramson Cancer Center) Job Profile Title Clinical more
    University of Pennsylvania (08/03/25)
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  • Field Clinical Specialist- Shockwave…

    J&J Family of Companies (Allentown, PA)
    …preferred but not required. + Working knowledge of clinical research, Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical ... trials. + A history of effective collaboration with regulatory agencies through clinical studies and market releases. + Product knowledge including product… more
    J&J Family of Companies (08/29/25)
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  • Medical Director/ Clinical Trial Physician…

    ThermoFisher Scientific (Allentown, PA)
    …of issues in consultation with the Global Medical Indication Lead + Interpret the clinical trial data for regulatory documents (eg CSR, INDs, Annual Reports, ... step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel… more
    ThermoFisher Scientific (08/13/25)
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  • Ambulatory Clinical Pharmacy Specialist,…

    Penn Medicine (Philadelphia, PA)
    …adherence to the hospital's medication use policies and procedures and relevant regulatory agencies. Clinical Pharmacy Specialists are foundational for providing ... 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 (08/26/25)
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  • Clinical Research Coordinator

    Actalent (Wynnewood, PA)
    …Conduct chart reviews and manage patient recruitment processes. + Pre-screen patients for clinical trials and manage regulatory documentation. + Enter and manage ... Job Title: Clinical Research CoordinatorJob Description We are seeking a...review and patient recruitment + Knowledge of GCP and regulatory requirements + Proficiency in data entry and EDC… more
    Actalent (08/19/25)
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  • Principal Scientist, Biostatistics

    Merck (North Wales, PA)
    …design, computing software and data management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase ... sound scientific principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions. This… more
    Merck (07/16/25)
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  • Senior Manager, Medical Writing

    Teva Pharmaceuticals (West Chester, PA)
    …Manager in Global Regulatory Medical Writing writes and edits clinical regulatory documents, including submission summaries and other complex documents. ... and fundamental accountability, provides strategic supervision, and planning assistance for clinical regulatory documents. + Writes and edits clinical more
    Teva Pharmaceuticals (08/09/25)
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