• Senior Solution Consultant

    Norstella (Trenton, NJ)
    …on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial landscape. Relying on us to deliver vital advantage when making ... from over 3000 of the world's leading pharmaceutical, contract research organizations (CROs), medical technology, biotechnology and healthcare service providers,… more
    Norstella (08/08/25)
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  • Clinical Support Representative

    Penn Medicine (Woodbury Heights, NJ)
    …mission of providing the highest level of care to patients, conducting innovative research , and educating future leaders in the field of medicine. Working for this ... items in appropriate location. + CSRs, if applicable as per regulatory guidelines: Maintains medication storage closet inventory and security; checks expiration… more
    Penn Medicine (08/07/25)
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  • VP, Deputy General Counsel, International

    Integra LifeSciences (Princeton, NJ)
    …in multiple jurisdictions and under a variety of complex legal and regulatory schemes; + Collaborating with the compliance team to ensure Integra's business, ... loans ; + Providing product counseling and guidance on commercial and regulatory affairs initiatives to ensure compliance with applicable laws and regulations; +… more
    Integra LifeSciences (07/31/25)
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  • Global Director, Medical Affairs

    Organon & Co. (Jersey City, NJ)
    …objectives. + Collaborate with cross-functional teams, including clinical development, regulatory affairs, marketing and sales, to ensure alignment of medical ... medical expertise and strategic guidance to support product development, regulatory submissions, and commercialization efforts. + Support business development… more
    Organon & Co. (07/24/25)
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  • Manager, Statistical Programming - REMOTE

    AbbVie (Jersey City, NJ)
    …a strategic role which guides a team of Statistical Programmers in the research and development of new pharmaceutical products. This role is directly responsible for ... must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations. Responsibilities: + Leads the statistical… more
    AbbVie (07/23/25)
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  • Medical Director, Global Medical Affairs, Early…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …for assigned areas. Knowledge and strong competency with the US healthcare system and regulatory landscape is required for this role. + Stay abreast of the latest ... advancements, research , and publications within the assigned disease areas in...evidence, US and global commercial teams, market access, and regulatory affairs, to ensure integrated global strategies and cohesive… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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  • Senior Hydrogeologist

    American Water (Camden, NJ)
    …wastewater disposal facilities to meet increasing and/or changing demands and regulatory requirements. * This includes supporting well and aquifer testing programs ... and Company standards for capacity, performance, reliability, safety and regulatory compliance. Serve as technical support during planning, construction,… more
    American Water (07/12/25)
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  • Commercial Credit Senior Associate

    M&T Bank (Iselin, NJ)
    …statements, monitoring loan portfolio, and ensuring compliance with credit policies and regulatory requirements. This client facing role serves as a critical link ... due diligence reports, credit bureaus, appraisals, internal credit information, industry research and peer data. Determine the need for more thorough investigation… more
    M&T Bank (07/11/25)
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  • Senior Counsel, Assistant Vice President of Legal…

    RWJBarnabas Health (West Orange, NJ)
    …+ Deep expertise in benefits contracting, health plan operations, and regulatory frameworks governing plan benefits + Demonstrated ability to negotiate high-stakes ... committees + Monitor and interpret federal and state legislative and regulatory developments affecting employee benefit plans, including ERISA, HIPAA, COBRA, MHPAEA,… more
    RWJBarnabas Health (07/04/25)
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  • Senior Principal Scientist, Development DMPK

    Bristol Myers Squibb (Princeton, NJ)
    …pharmacokinetics activities of multiple projects; be responsible for preparation of regulatory dossier / submissions; and assist in developing strategy for the ... DSUR, etc. to support clinical trials and global registrations. Interacts with regulatory authorities to address questions as needed. + Support clinical assets for… more
    Bristol Myers Squibb (06/29/25)
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