• Senior Director, Global Medical Oncology, IO…

    Bristol Myers Squibb (Princeton, NJ)
    …broad cross functional matrixed partners in their work to ensure optimal medical affairs strategy is developed and executed. This senior medical leader will report ... + Develop and execute the WW & US Medical Affairs strategy for key assets. + Act as the...work effectively with cross functional teams including clinical, commercialization, regulatory , HEOR and Access. + Excellent strategy development, critical… more
    Bristol Myers Squibb (11/24/25)
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  • Sr Director, Medical Education and Programs

    Gilead Sciences, Inc. (Parsippany, NJ)
    …Senior Director will collaborate with cross-functional teams (eg Legal, Compliance, Public Affairs , and Medical Affairs colleagues) to develop and implement ... integrated strategies that align with the Medical Affairs goals while ensuring compliance with ACCME, FDA, OIG,...statutes and regulations). Staying abreast of industry trends and regulatory changes in the medical education is crucial to… more
    Gilead Sciences, Inc. (10/07/25)
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  • Director, Global Medical Oncology, US IO Lung…

    Bristol Myers Squibb (Princeton, NJ)
    …budget utilization. + Partner closely with colleagues in Discovery, Clinical Research, Regulatory , and Health Outcomes to ensure the science of the pipeline products ... MD, PhD, PA/NP) + Prior (5+ years) pharmaceutical industry experience in medical affairs is preferred + Highly organized and motivated individual with the ability to… more
    Bristol Myers Squibb (11/26/25)
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  • Senior Manager, IT Web Services

    Sumitomo Pharma (Trenton, NJ)
    …This includes websites supporting Marketing, Corporate Communications, and Medical Affairs . The ideal candidate combines front-end development expertise with ... Partner with business stakeholders across Marketing, Corporate Communications, and Medical Affairs to gather requirements, propose solutions, and ensure align with… more
    Sumitomo Pharma (11/13/25)
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  • Vice President, Head of Neuropsychiatry Late…

    J&J Family of Companies (Titusville, NJ)
    …work with the CDTL, DAS lead and with functional partners from global medical affairs , health care compliance, legal regulatory , and other relevant groups. + The ... and for final protocols, clinical study reports, and clinical components of regulatory packages/submissions. He or she may delegate some of these responsibilities,… more
    J&J Family of Companies (10/30/25)
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  • Associate Director, Statistics - Immunology

    AbbVie (Florham Park, NJ)
    …areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... of a team. Lead/develop statistical strategy for project development and regulatory submission. + Provide statistical leadership for design, analysis and reporting… more
    AbbVie (10/15/25)
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  • Associate Director, ICSR Management Team - Job ID:…

    Ascendis Pharma (Princeton, NJ)
    …create Corrective Action and Preventative action (CAPA) as applicable. + Oversee regulatory and departmental compliance by ensuring timely processing of ICSRs in the ... SOPs, Work Instruction etc. as applicable and ensure compliance with regulatory guidelines and regulations. + Responsible for identifying and developing training… more
    Ascendis Pharma (10/09/25)
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  • Senior Counsel (Medical Device)

    Fujifilm (Trenton, NJ)
    …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or operating divisions, under the ... Division General Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to… more
    Fujifilm (09/04/25)
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  • Director, WW Medical Cardiovascular & Immunology,…

    Bristol Myers Squibb (Princeton, NJ)
    …Strategy within WW Medical Cardiovascular & Immunology (CV & I) Global Medical Affairs , and is responsible for assisting with early medical and scientific strategy ... resource allocation and prioritization of projects. + Collaborate with R&D, Commercial, Regulatory , and other key functions to ensure seamless execution of portfolio… more
    Bristol Myers Squibb (11/26/25)
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  • Senior Manager, Medical Content Product Manager-…

    Bristol Myers Squibb (Princeton, NJ)
    …acceptance criteria. + Prioritize and groom the backlog to balance regulatory compliance, business value, risk, and technical feasibility; run effective PI/iteration ... facilitating risk assessments. + Strong stakeholder leadership across Medical Affairs , Medical Information, Field Medical, Compliance/QA, Architecture, and Engineering;… more
    Bristol Myers Squibb (11/26/25)
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