• Director R&D Program Management

    Abbott (Pleasanton, CA)
    …work closely with cross-functional peers in quality, operation, marketing, clinical and regulatory , medical affairs , commercials to define an aligned and ... protected. + Interfaces with appropriate internal and external resources ( regulatory , customers, etc.) to ensure development programs meet regulatory more
    Abbott (08/13/25)
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  • Senior Scientific Director , Clinical…

    AbbVie (Irvine, CA)
    …opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues.… more
    AbbVie (08/08/25)
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  • Senior Director , Auditing, Monitoring…

    Centene Corporation (Raleigh, NC)
    …and coordinates with Internal Audit, Regulatory Compliance and/or Market based Regulatory Affairs on responses to agency inquiries and oversees the internal ... issues and implementation of new compliance requirements with respect to regulatory and contractual language + Conducts compliance reviews and manages team… more
    Centene Corporation (07/05/25)
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  • Associate Director , Statistics, Medical…

    Otsuka America Pharmaceutical Inc. (Boise, ID)
    …data scientists and data programmers, and external stakeholders including Medical Affairs , Value and Real World Evidence to provide end-to-end statistical expertise ... approve tables, listings and graphs specifications. + Closely work with Medical Affairs to support statistical design, conduct secondary analyses of clinical and… more
    Otsuka America Pharmaceutical Inc. (09/05/25)
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  • Associate Director , Social Media Strategy

    Gilead Sciences, Inc. (Foster City, CA)
    …**Stakeholder Engagement & Enablement** + Coordinate with internal teams (Public Affairs , Marketing, HR, Business Units) to source content and amplify enterprise ... stakeholders at all levels. **Preferred:** + Background in public affairs , corporate communications, reputation management, consulting, PR agencies or government… more
    Gilead Sciences, Inc. (09/05/25)
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  • Associate Director , Medical Writer…

    BeOne Medicines (Emeryville, CA)
    …health economic and outcomes research in the oncology space + Familiarity with global regulatory and medical affairs environments (eg, US, EU, APAC) + Experience ... lead the tactical execution of publications stemming from our global medical affairs publication plans. These plans span across early phase development to marketed… more
    BeOne Medicines (07/16/25)
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  • NERC Regulatory Compliance Expert II

    Duquesne Light Company (Pittsburgh, PA)
    …plans are put in place and completed on schedule. Work closely with the Director NERC Compliance, the Regulatory Compliance Senior Managers and business unit ... processes, business units and oversight responsibilities. Responsible for assisting the Regulatory Compliance Senior Managers with NERC CIP and O&P compliance… more
    Duquesne Light Company (08/09/25)
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  • Senior Director , Quality, Digital

    GE HealthCare (Bellevue, WA)
    …Computer Science or equivalent. + Minimum 10 years' experience in Quality Assurance / Regulatory Affairs . + Minimum of 2 years' experience as a people leader. ... for the business and driving Quality metrics. Ensures quality and regulatory compliance while driving process effectiveness and efficiency. Represents GE HealthCare… more
    GE HealthCare (09/13/25)
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  • Director of Quality Control

    Jabil (Hunt Valley, MD)
    …programs are maintained. + Collaborate with colleagues in Research & Development, Regulatory Affairs , Quality Assurance, and external partners and vendors or ... or established in the laboratory conform to current and appropriate scientific and regulatory standards are suitable for use for their intended purpose. + Develop… more
    Jabil (09/11/25)
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  • Oncology Early Stage Clinical Scientist…

    Pfizer (South San Francisco, CA)
    …and external partners, such as project leaders, research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational oncology, ... clinical study reports (CSRs), investigator brochures, statistical analysis plans, and regulatory documents. + Foster a transparent environment that builds strong… more
    Pfizer (08/21/25)
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