• Sun Pharmaceuticals, Inc (Princeton, NJ)
    …market with a focus on dermatology, ophthalmology and onco-dermatology. **Job Summary:** Scientist II , MSTG, performs process development studies, Exhibit batch ... execution of DOEs, process optimization studies, and process qualification batches, Process data compilation and data analysis using statistical tools. + Develop… more
    DirectEmployers Association (09/03/25)
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  • Audit Manager II -Enterprise Risk…

    City National Bank (Jersey City, NJ)
    …requests for advanced analytics by providing detailed and clear questions to the Data Analytics Lead or Data Scientist .Applies advanced analytical techniques ... *AUDIT MANAGER II - ENTERPRISE RISK MANAGEMENT* WHAT IS THE OPPORTUNITY?...auditors to assess risks, develop detailed audit programs, identify data analytic opportunities, execute audit programs, analyze results of… more
    City National Bank (10/16/25)
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  • Director, Early Clinical Development - Immunology…

    Bristol Myers Squibb (Madison, NJ)
    …medical accountability and oversight for multiple clinical trials + Manages Phase I/ II studies, with demonstrated decision making capabilities + Provides medical and ... clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal functional author for… more
    Bristol Myers Squibb (10/18/25)
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  • Associate Director, Oncology Clinical Biomarker…

    Bristol Myers Squibb (Princeton, NJ)
    …Seeking candidates with Biomarker Lead late stage clinical trials for Phases II /III preferred. Regulatory submissions drug approvals in solid tumor space also highly ... of this role are to act as a lead scientist to implement and deliver on biomarker strategies for...for clinical programs, develop reports and publications on translational data generated to support asset development and contribute to… more
    Bristol Myers Squibb (10/28/25)
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  • Director, Study Responsible Physician - Mivexian

    J&J Family of Companies (Raritan, NJ)
    …responsible for site interactions in partnership with the clinical project scientist (CPS) for medical questions and education (including safety management ... approval of essential documents for regulatory filings. Performs medical safety data review, including evaluation of adverse events and eligibility of participants… more
    J&J Family of Companies (10/23/25)
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