• Associate Director, Promotional Materials

    Taiho Oncology (Princeton, NJ)
    …principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working ... 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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  • Business Analyst Manager, SSDM

    Sanofi Group (Morristown, NJ)
    …as well as the Information Technology (ITS) department. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve ... required. + In-depth knowledge of International pharmacovigilance requirements/ EU, FDA requirements/international guidelines, ICH/CIOMS, with experience in their practical… more
    Sanofi Group (07/25/25)
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  • Clinical Services Coordinator

    Penn Medicine (Voorhees, NJ)
    …self and assigned area(s) are compliant with all applicable federal, state, and local regulatory standards (ex OSHA, TJC, DOH, FDA , HIPAA, etc.) + Oversees the ... + Clinical Care Associates (CCA) MAs, if applicable as per regulatory guidelines: administers prescribed medications, gives injections and vaccines; reads PPD… more
    Penn Medicine (08/20/25)
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  • Quality Assurance Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …chance to do important work that creates change and shapes the future of healthcare . Thinking differently is what we do best. To us, change equals opportunity. Every ... Device Directive, the Canadian Medical Device Regulations (CMDR), and other applicable regulatory agencies. The QA Engineer II will collaborate with site NC… more
    Integra LifeSciences (08/17/25)
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  • Senior Director, CNS Communications

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …understanding of important topics including clinical trial design, drug development, regulatory decision making and public policy. + Responsible for comprehensive ... education programs, as well as planning around key data announcements, regulatory milestones and launch planning for late-stage pipeline candidates. + Maintain… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Senior Director, Communications,…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …understanding of important topics including clinical trial design, drug development, regulatory decision making and public policy. . Responsible for comprehensive ... education programs, as well as planning around key data announcements, regulatory milestones and launch planning for late-stage pipeline candidates. . Maintain… more
    Otsuka America Pharmaceutical Inc. (07/26/25)
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  • Director, PV Medical Surveillance

    Taiho Oncology (Princeton, NJ)
    …principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working ... concerns and risk/benefit profile for responsible compounds, as well as regulatory guidelines as they pertain to drug safety/pharmacovigilance. + Responsible for… more
    Taiho Oncology (07/12/25)
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  • Senior Supervisor, QA Microbiology

    J&J Family of Companies (Raritan, NJ)
    At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, ... we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact… more
    J&J Family of Companies (08/16/25)
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  • Senior Manager, Medical Affairs Communications…

    Belcan (Whippany, NJ)
    …and internal use. * Collaborate with cross-functional teams including Medical Affairs, Regulatory , and Legal to review and help ensure scientific accuracy and ... medical information. Required Qualifications (Senior Manager Level): * Advanced degree in a healthcare discipline (PharmD, MD, PhD) * 1-2 years of experience in the… more
    Belcan (08/27/25)
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  • Mammography Technologist

    RWJBarnabas Health (Lakewood, NJ)
    …routine and advanced mammography procedures within the scope defined by regulatory and departmental standards. Qualifications: Required: + ARRT Certification in ... in maintaining current continuing education credits as required by the FDA /MQSA and ACR Preferred: + Previous Mammography experience Scheduling Requirements: +… more
    RWJBarnabas Health (08/25/25)
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