• GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …and clinical performance studies.Ability to synthesize and critically analyze data from multiple sources. + **Collaboration Skills:** Ability to work effectively ... information can be found through the LINK (https://benefits.sanofiusallwell.com/fleet/public/index/ba511bf8-5c32-4828-9861-ab985fffab90/?cid=sanofi) . Global Terms & Conditions and Data Privacy… more
    Sanofi Group (09/20/25)
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  • Manager/Senior Manager - R&D SME

    Axtria, Inc. (Berkeley Heights, NJ)
    Introduction Axtria is a leading global provider of cloud software and data analytics to the Life Sciences industry. We help Life Sciences companies transform ... value. Key Responsibilities + Domain Leadership: Serve as the R&D/ Clinical expert for data onboarding and governance....analytics and insights. + Apply deep knowledge of pharma data governance, access management, and compliance standards more
    Axtria, Inc. (11/14/25)
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  • Senior Director, Medical Communications CNS

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    global publication plan for CNS assets, ensuring successful presentation of clinical data at major international congresses and in peer-reviewed journals + ... Collaborate with the CNS Medical BU Lead and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory, Commercial)… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Director, Early Precision Medicine Regulatory…

    Bristol Myers Squibb (Princeton, NJ)
    …with deep expertise in assay and IVD development-including analytical validation, clinical development, manufacturing, and global regulatory submissions through ... apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of… more
    Bristol Myers Squibb (12/03/25)
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  • Director Biostats Real World Evidence

    Bristol Myers Squibb (Princeton, NJ)
    …and establish priorities + Strong understanding of healthcare industry regulatory compliant data standards . **Why You Should Apply** Around the world, we ... to inform evidence generation, supporting developing clinical program design, clinical trial execution, and other data -driven decision-making activities. The… more
    Bristol Myers Squibb (12/08/25)
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  • Senior Scientist, Statistical Programmer- Hybrid

    Merck (Rahway, NJ)
    …CDISC SDTM and ADaM standards + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH + Designs ... drugs and vaccines for the benefit of patients and global human health. This position provides high quality statistical...Specific Required Skills and Experience:** + Programming expertise with clinical endpoint data (efficacy and safety) and… more
    Merck (12/06/25)
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  • Senior Director, Medical Communications,…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …publication plan for Nephrology & Immunology assets, ensuring successful presentation of clinical data at major international congresses and in peer-reviewed ... with the Nephrology & Immunology BU Lead and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory, Commercial)… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Manager, Medical Core Content - Rare Disease

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …approved core scientific narrative and lexicon, accurately reflects clinical trial data , and maintains consistency across global materials + Maintain content ... and production of scientific assets, ensuring they accurately reflect clinical data , adhere to the core scientific...repositories and ensure version control and accessibility for global teams + Utilize platforms like Veeva Vault, to… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Security Architecture Specialist - AI & Regulated…

    Oracle (Trenton, NJ)
    …HDI's software, AI systems, data flows, and infrastructure meet strict global standards for security, privacy, MDR compliance, and AI safety. ... MDR (Medical Device Regulation), AI regulatory requirements, and emerging global security standards , we are expanding our...clinical data systems. + Experience with data privacy standards (GDPR, HIPAA, CCPA). +… more
    Oracle (12/05/25)
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  • Virology (HIV) Regional Medical Scientific…

    Merck (Trenton, NJ)
    …reports to the Regional RMSD Team Leader - within US Medical Affairs, Global Clinical Development, Research and Development (R&D). **Location details:** + This ... Communicate external stakeholder opinions, insights and feedback on new data , clinical trends and the evolving vaccine...+ Develop and execute territory plans in alignment with global Virology strategy + Support data generation… more
    Merck (12/09/25)
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