• Global Development Lead, Medical Director,…

    Pfizer (Collegeville, PA)
    …and management of clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + ... working in a matrix team environment with other clinicians, statisticians, clinical pharmacologists, translational biologists and regulatory specialists. Meet… more
    Pfizer (08/08/25)
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  • Associate Practice Manager - Cancer Ctr VF

    Penn Medicine (Berwyn, PA)
    …supervision and direction in regards to all administrative, financial, regulatory , quality, human resources, patient/employee satisfaction, and clinical ... (research initiatives, resident program), special clinical programs, multiple clinical specialties, complex regulatory requirements, management of external… more
    Penn Medicine (08/07/25)
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  • Digital Product Portfolio Head

    ThermoFisher Scientific (Allentown, PA)
    …Office **Job Description** Thermo Fisher Scientific Inc. is the world leader in serving science , with annual revenue of more than $40 billion. Our Mission is to ... Unity Lab Services, Patheon and PPD. The PPD (TM) clinical research business of Thermo Fisher Scientific is a...building new products that spans study start to final regulatory delivery. This role is responsible for leading Product… more
    ThermoFisher Scientific (08/17/25)
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  • Dir, Engineering, CMC Leader for Biologics

    Merck (West Point, PA)
    …mitigates risks across all factors that may impact technical, operational & regulatory success or timelines. Analyzes and develops innovative solutions to unforeseen ... circumstances. + Responsible to ensure the best science and most robust processes are used, working closely with DCRC. As the Product TPL takes ownership for the… more
    Merck (08/08/25)
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  • Quality Assurance Auditor II

    Charles River Laboratories (Wayne, PA)
    …of a variety of processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. In the ... review of study and QA files in preparation for sponsor site visits and regulatory inspections; assure that QA audit files are retained. + Host client site visits… more
    Charles River Laboratories (08/21/25)
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  • Therapeutic Medical Physicist

    Veterans Affairs, Veterans Health Administration (Pittsburgh, PA)
    …Medical Physicist (Advanced Level) The TMP provides professional, scientific, and clinical practice of therapeutic medical physics for external beam radiotherapy and ... of new radiotherapy techniques and modalities. Advanced knowledge of regulatory requirements, manufacturer's standards, and professional society guidelines for… more
    Veterans Affairs, Veterans Health Administration (07/31/25)
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  • Warehouse Technician II

    Kelly Services (West Point, PA)
    …that may be available to you as a member of the Kelly Talent Community. Why Kelly (R) Science & Clinical ? Kelly Science & Clinical is your connection to ... Transportation Management, Material Receipts and Warehouse Operations. Adherence to regulatory , global and site policies and procedures governing operations… more
    Kelly Services (08/11/25)
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  • Associate Director, Quantitative Pharmacology…

    Merck (West Point, PA)
    …n/a **Required Skills:** Clinical Development, Clinical Pharmacology, Clinical Trial Designs, Data Modeling, Data Science , Data Visualization, Drug ... cross-functional teams of experienced scientists to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and ophthalmologic… more
    Merck (08/21/25)
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  • Director, Prospective + Concurrent Risk Adjustment…

    Datavant (Harrisburg, PA)
    …of product managers and product designers and collaborate deeply with data science , clinical experts, engineering, and commercial teams to accelerate innovative ... solutions that surface timely, high-accuracy clinical insights directly into provider workflows. These capabilities help health plans and risk bearing groups improve… more
    Datavant (08/08/25)
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  • Principal Scientist, Engineering - Biologics, Drug…

    Merck (West Point, PA)
    …transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group ... is responsible for establishing the science , engineering and knowledge required for today's innovative and...and qualification (PPQ) and shelf-life strategies. + Influences CMC regulatory strategy and is accountable for DP CMC sections… more
    Merck (08/08/25)
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