• Oncology Early Stage Clinical Scientist (Director,…

    Pfizer (Collegeville, PA)
    …clinical study reports (CSRs), investigator brochures, statistical analysis plans, and regulatory documents. + Foster a transparent environment that builds strong ... external partners, such as project leaders, research units, biostatistics, regulatory affairs, clinical pharmacology, human genetics, translational oncology, precision… more
    Pfizer (08/21/25)
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  • Senior Principal Scientist, Clinical Research,…

    Merck (North Wales, PA)
    …development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may ... Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects… more
    Merck (08/20/25)
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  • Quantitative Analytics and Model Development Group…

    PNC (Pittsburgh, PA)
    …testing frameworks, and compliance with Basel, CCAR, IRRBB and Liquidity Risk regulatory framework. This highly visible role reports directly to the Chief Market ... approves the preparation and analysis of detailed documents for validation and regulatory compliance. + Directs, motivates, develops and manages the performance of… more
    PNC (08/17/25)
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  • Head of Data Governance Capabilities…

    PNC (Pittsburgh, PA)
    …high-quality data is available and accessible to power analytics, regulatory reporting, AI/ML, and operational decision-making. Other primary responsibilities ... policies, standards, and frameworks aligned with business goals and regulatory requirements. *Design and implement scalable data quality frameworks, including… more
    PNC (08/13/25)
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  • Director, Packaging Distribution, Components…

    Merck (West Point, PA)
    …substance and drug product container closure systems including mold qualification and regulatory compliance. To act as master data stewards and support enterprise ... commercialization teams across the end to end supply chain, and analytical, regulatory , and project leaders. The successful candidate will demonstrate ownership and… more
    Merck (08/12/25)
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  • Associate Director - CMC Development

    Lilly (Philadelphia, PA)
    …Development, Analytical Sciences, Manufacturing, Quality, Supply Chain, R&D, Finance, and Regulatory to ensure delivery of CMC milestones for priority assets ... with senior management and across relevant functional areas. + Support regulatory strategy development and health authority interactions related to CMC; Drive… more
    Lilly (08/12/25)
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  • Director, Engineering Assembly and Packaging…

    Merck (West Point, PA)
    …development and technology teams, supply chain, operations, quality, analytical, regulatory , and project leaders. The successful candidate will demonstrate ownership ... relationships with internal stakeholders, including packaging commercialization, quality, analytical, regulatory , manufacturing, Device Development and Technology, Technical Product Leaders,… more
    Merck (08/12/25)
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  • Risk & Control Director

    PNC (Pittsburgh, PA)
    …governance, policies, and oversight - Experience supporting or responding to regulatory requests, including familiarity with financial prudential agencies (eg, OCC, ... and enhanced to support the businesses in managing their risks while meeting regulatory expectations. + Oversees the timely and proper execution of the risk… more
    PNC (08/02/25)
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  • Senior Tax Manager

    PNC (Pittsburgh, PA)
    …accuracy of reported results and provide expertise in all financial statement and regulatory reporting matters. The Senior Tax Accounting Manager reports to the Tax ... and review of the income tax portion of the regulatory reporting process including projections of income tax expense...degree. Higher level education such as a Masters degree, PhD , or certifications is desirable. Industry experience is typically… more
    PNC (07/31/25)
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  • Senior Director, Global Clinical Development CNS

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the ... + Formulating a rationale to develop the drug in accordance with a clinical and regulatory strategy. + Working with experts and consultants in the field to refine a… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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