• Senior Medical Science Liaison

    Cardinal Health (Trenton, NJ)
    …across multiple functions and within a region to maximize theranostic knowledge and clinical strategies + Lead scientific strategy at medical congresses + ... hospitals within three hours. We also provide customers the support they need in regulatory compliance, reimbursement, continuing education,...Lead internal and external clinical education programs + Provide timely… more
    Cardinal Health (08/15/25)
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  • Global Project Head, Rare

    Sanofi Group (Morristown, NJ)
    …and communication plans with Commercial and Investor Relations. + Direct management clinical lead . + Matrix leadership and dotted-line management toward all ... team in achieving corporate goals. The GPH establishes the goals and will support staff within the program and participates in strategic planning for, and oversight… more
    Sanofi Group (07/30/25)
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  • Director Materials/ Support Mgmt

    Hunterdon Health Care System (Flemington, NJ)
    …Reporting Relationships ? Reports to: o Assistant Vice President Operations, Decision Support ? Supervises: Assistant Director Materials Management, OR ... meeting annual goals and objectives, to include performance related to finance, clinical activity, quality, safety, marketing, and human resources 7. Actively seeks… more
    Hunterdon Health Care System (06/13/25)
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  • TA Head of Biostatistics, Neuroscience…

    Sanofi Group (Morristown, NJ)
    …Biostatistics.** You will be leading and overseeing all statistical work for clinical development and regulatory submissions, leading a team focused on clinical ... influential and collaborative role, the Biostatistics TA Head partners closely with clinical teams, Clinical Sciences & Operations (CSO), regulatory experts, and… more
    Sanofi Group (07/18/25)
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  • Scientific Director/Senior Scientific Director,…

    Bristol Myers Squibb (New Brunswick, NJ)
    …management, we provide valuable project information and portfolio insights, and we lead CMC due diligence for business development opportunities. Joining PSI means ... and encompass drug substance, drug product, analytical, quality, regulatory, and clinical supplies. + Represents the Global Product Development and Supply (GPS)… more
    Bristol Myers Squibb (08/30/25)
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  • Director, Integrated Publications

    Taiho Oncology (Princeton, NJ)
    …to improving patient outcomes. Position Summary: The. Director will be accountable and lead the development of the publications plan ( clinical and EVD), across ... /Posters/ oral presentations and slide loops development across the portfolio. + Provide support to product medical leads, EVD lead , Medical Information and… more
    Taiho Oncology (07/25/25)
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  • Solutions Architect

    Evolent (Trenton, NJ)
    …development is preferred + **Experience with SMART on FHIR** applications, CDS Hooks, and clinical decision support systems is preferred + **Background in ... across multiple specialties + Implement real-time data synchronization that enables timely clinical decision -making ** Lead Technical Excellence** + Provide… more
    Evolent (06/26/25)
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  • Strategic Customer Director - Mid-market - North…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …departments, and develop impactful concepts that enhance customer experience. + Relationship Lead : Gain access to executive and enterprise-level decision makers, ... health systems (IDNs). The SCD will represent the entire BD portfolio and lead a multi-functional matrix team consisting of sales, business unit national accounts, … more
    BD (Becton, Dickinson and Company) (08/02/25)
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  • Associate Director, Global Regulator Strategy,…

    Bristol Myers Squibb (Princeton, NJ)
    …Responsibilities:** + Support the preparation of, and participate in / lead (as appropriate), key HA interactions. Assure consistent positions on common issues ... for global regulatory strategy within a development team (DT). Serve as team lead or co- lead of marketing application submission teams for indications that… more
    Bristol Myers Squibb (08/30/25)
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  • Director, GCP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …and follow up on CAPAs to ensure timely resolution and CAPA effectiveness. + Lead / Support risk assessment activities, in partnership with risk program and SMEs. ... deliverables across large sites, countries, or multiple regions. + Lead internal and external R&D quality audits for assigned...Audit related CAPAs. + Stay current with evolving global clinical regulations and guidance. + Support the… more
    Gilead Sciences, Inc. (08/21/25)
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