• Associate Director Value and Access…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Associate Director Value and Access Flu and Covid- Vaccines **Location:** Morristown, NJ **About the Job** Drive excellence in coverage and ... of CMS regulations for vaccine payment + Strong understanding of legal, regulatory , and compliance reimbursement requirements + Demonstrated ability to influence key… more
    Sanofi Group (07/16/25)
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  • Associate Director , Promotional…

    Taiho Oncology (Princeton, NJ)
    …the promotional and medical materials review committees. Position Summary: ​​ The Associate Director , Promotional Materials will provide guidance to the ... teams regarding communications strategy and planning. + Review and approve the regulatory content of materials created for product promotion, corporate, and other… more
    Taiho Oncology (07/04/25)
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  • Associate Director , Marketing

    Merck (Rahway, NJ)
    …medicines that help people around the globe. We are currently recruiting for Associate Director , US Marketing The role will oversee foundational strategy and ... to drive and align on decisions, including field sales, marketing operations, Legal, Regulatory , Medical, etc. Our US marketing team has adopted an Agile operating… more
    Merck (06/08/25)
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  • Associate Medical Director

    Evolent (Trenton, NJ)
    …mission. Stay for the culture. **What You'll Be Doing:** Evolent is seeking an ** Associate Medical Director - Cardiovascular Medicine** to play a critical role ... and expedited appeals,** ensuring compliance with UM policies and regulatory requirements. + Collaborate with cross-functional teams, including **clinical reviewers,… more
    Evolent (06/03/25)
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  • Associate Director , Omnichannel…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …to optimize omnichannel marketing campaigns. You will report to the Sr Director , Omnichannel Advanced Analytics Lead. This role is dynamic, fast-paced, highly ... managed, governed, and secured, following industry best practices and regulatory requirements. + Model Otsuka's core competencies (Accountability for Results,… more
    Otsuka America Pharmaceutical Inc. (07/31/25)
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  • Associate Director , Oncology…

    Bristol Myers Squibb (Princeton, NJ)
    …on translational data generated to support asset development and contribute to regulatory submissions. This individual will work on cross-functional project teams to ... scientists, as well as BMS members from clinical, medical, commercial, regulatory , and diagnostics. Individual will also engage with external academic… more
    Bristol Myers Squibb (08/09/25)
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  • Associate Director , Environmental…

    Bristol Myers Squibb (Princeton, NJ)
    …fate/effects studies and environmental risk assessments according to appropriate international regulatory guidelines. This role will lead and participate on diverse ... risk assessments and environmental fate/effects studies focused on global regulatory frameworks, technical knowledge and emerging scientific trends; Lead matrix… more
    Bristol Myers Squibb (07/18/25)
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  • Associate Director , Health Physics

    Bristol Myers Squibb (Princeton, NJ)
    …NJDEP. + Serve as the Cyclotron Particle Accelerator Safety Officer (PASO). Regulatory qualifications/requirements to be eligible as a PASO are noted in ... use, training, and disposition of all X-ray generating devices. Included regulatory requirements and responsibilities such as registrations, surveys, operations, and… more
    Bristol Myers Squibb (07/13/25)
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  • Associate Director , Medical Affairs…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …through commercial launch-ensuring all products meet rigorous safety, efficacy, and regulatory standards. + Clinical Risk Assessment: Collaborate with the Global ... and advertising materials to ensure clinical accuracy and compliance with regulatory standards. + Work collaboratively with R&D, Marketing, Business Development, and… more
    BD (Becton, Dickinson and Company) (06/29/25)
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  • Associate Director , Neuroimmunolgy…

    Bristol Myers Squibb (Princeton, NJ)
    …activities for the pipeline and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development drives ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… more
    Bristol Myers Squibb (08/08/25)
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