• Director , Global Regulatory

    Merck (North Wales, PA)
    **Job Description** The Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global ... business standards, process maps, and risk management for global processes across Global Regulatory Affairs and Clinical Safety . The Global Process… more
    Merck (01/10/25)
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  • Associate Director , Regulatory

    Merck (West Point, PA)
    …Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late Development (AdVAnce) ... utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings. As the AdVAnce facility will not be fully constructed and… more
    Merck (12/12/24)
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  • Director , Corporate Affairs

    Merck (West Point, PA)
    **Job Description** **Job Scope** The Director , Corporate Affairs and Patient Innovation & Engagement Compliance has global compliance responsibility for all ... areas of Corporate Affairs , including Global Communications, Global and Regional Public Policy,...Research and Development Division's Value & Implementation organization. The Director serves as a dedicated global business… more
    Merck (01/18/25)
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  • Chief Of Staff, Executive Director

    Olympus Corporation of the Americas (Center Valley, PA)
    …it is likely not legitimate._ **Job Description** The Chief Of Staff, Executive Director Global QARA Strategic Projects position is two-fold. The first is ... second is to help investigate, analyze, and create holistic global plans to resolve current critical Regulatory ...Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs more
    Olympus Corporation of the Americas (01/25/25)
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  • Medical Director /Senior Medical…

    J&J Family of Companies (Spring House, PA)
    …applications. Other functional groups represented on the team include project management, regulatory affairs , global clinical operations, data management, ... to the implementation of clinical research studies that are part of a global compound development program. The Medical Director /Senior Medical Director more
    J&J Family of Companies (01/22/25)
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  • Medical Director , Late Development,…

    Pfizer (Collegeville, PA)
    …The medical director works closely with other functions such as regulatory affairs , pharmacovigilance, biostatistics, and medical affairs to ensure ... that the clinical development program meets the scientific, ethical, and regulatory standards. The medical director also provides medical expertise and guidance… more
    Pfizer (01/22/25)
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  • Clinical Director , Oncology Early…

    Merck (Upper Gwynedd, PA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** Our company is a global health care leader with a diversified portfolio...of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director more
    Merck (01/16/25)
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  • Executive Director , Design Assurance

    Olympus Corporation of the Americas (Center Valley, PA)
    …other functions and strategic partners such as R&D, Manufacturing, Medical Safety, and Regulatory Affairs to establish, drive, and achieve excellence in product ... and oversee the following processes in support of the Global Design Assurance team: + Oversight over the ...Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs more
    Olympus Corporation of the Americas (12/19/24)
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  • Senior Director , Clinical Research,…

    Merck (North Wales, PA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director more
    Merck (12/08/24)
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  • US Specialty Care Medical Lead

    Pfizer (Collegeville, PA)
    … and Field Medical Outcomes organizations + Maintains strong working relationships with Global Medical Affairs Leads, Outcomes & Evidence, Clinical Sciences, PRD ... to have a thorough understanding of the processes associated with Medical Affairs . Working knowledge of lifecycle management and regulatory processes is… more
    Pfizer (01/18/25)
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  • VP, US Field Medical Lead

    Pfizer (Collegeville, PA)
    …and IM priority therapeutic areas. This role partners cross-functionally with US Brand Medical, Global Medical Affairs , Global Health and Value, Research & ... Lead is responsible for leading the US Field Medical Director (FMD) and Field Medical Outcomes (FMO) organization across...(or analougous group) + Maintains strong working relationships with Global Medical Affairs Leads, US Medical … more
    Pfizer (01/18/25)
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  • Distinguished Scientist, Product Development Team…

    Merck (North Wales, PA)
    …a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing to ... (Executive Director ) and Product Development Team (PDT) lead, Oncology Global Clinical Development, has primary responsibility for the planning and directing… more
    Merck (12/19/24)
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  • Medical Safety Specialist II

    Olympus Corporation of the Americas (Center Valley, PA)
    …Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs , Research & Development, Legal, and Health ... areas. You will report directly to the Medical Safety Director as a member of the global ...806, 820), various standards (GCP, ISO 13485, ISO 14971), regulatory filings (FDA IDE, 510K, EU-MDR CERs, SSCP, PMCFs,… more
    Olympus Corporation of the Americas (01/09/25)
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  • Senior Principal Scientist, Thoracic Malignancies

    Merck (North Wales, PA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director more
    Merck (12/17/24)
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  • Principal Scientist, Clinical Research, GYN…

    Merck (North Wales, PA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
    Merck (01/16/25)
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  • Principal Scientist, Translational Medicine

    Merck (West Point, PA)
    …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
    Merck (12/21/24)
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