• Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Trenton, NJ)
    clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contributes ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data )… more
    Sumitomo Pharma (10/11/25)
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  • Senior Principal Applied Scientist

    Oracle (Trenton, NJ)
    …Hugging Face Transformers, TensorFlow, or PyTorch. + Strong understanding of multi-modal data integration, clinical interoperability standards (FHIR, HL7), ... **Job Description** Oracle Health Data Intelligence (HDI) is at the forefront of...Oracle's AIDP platform to solve population health, research, and clinical interoperability challenges at global scale. +… more
    Oracle (11/25/25)
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  • Associate Principal Scientist, Statistical…

    Merck (Rahway, NJ)
    …to be programmed, an understanding of statistical terminology and concepts. + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... **:** + Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good… more
    Merck (12/02/25)
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  • Senior Statistical Programmer- Analysis…

    Merck (Rahway, NJ)
    …and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the ... Specific Required Skills and Experience:** + Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH +… more
    Merck (12/06/25)
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  • 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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  • Sr. Scientist, Statistical Programmer, Late Stage…

    Merck (Rahway, NJ)
    …to be programmed; an understanding of statistical terminology and concepts + Familiarity with clinical data management concepts + Experience in CDISC and ADaM ... Activities:** + Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good… more
    Merck (12/02/25)
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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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  • US Medical Director, Dupilumab Atopic Dermatitis

    Sanofi Group (Morristown, NJ)
    …not limited to FDA, OIG, DDMAC/OPDP,PhRMA,ICMJE,ISPOR). + Oversee conduct of all clinical studies in adherence to both Company standards , and government/industry ... to applicable SOP(s). + Partner with US Drug Safety in the management of clinical trial adverse events, post-marketing safety data , and in the communication of… more
    Sanofi Group (12/12/25)
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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 (12/11/25)
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