• Clinical Development Lead, Neuropsychiatry (Senior…

    Bristol Myers Squibb (Madison, NJ)
    …Collaborates with Global Development Operations/Global Compliance Group to develop asset level risk management plan, resolves issues with Quality/CS, and raises ... as necessary + Accountable in partnership with the Clinical Scientist for the design, execution, and analyses of each...Patient Safety physicians in the ongoing review of safety data + Serves as the (co-)leader of the cross-functional… more
    Bristol Myers Squibb (11/11/25)
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  • Senior Clinical Trial Physician, Rheumatology

    Bristol Myers Squibb (Princeton, NJ)
    …Lead - provides guidance and training to new CTP (not limited to data management ; systems training), therapeutic training, innovative study design and sets ... insights into biology, translational elements, as well as overall benefit risk assessments. This role includes support of cross-portfolio activities in line… more
    Bristol Myers Squibb (11/19/25)
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  • Manager, PVRM

    Sumitomo Pharma (Trenton, NJ)
    …not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties ... regulations and drug safety reporting requirements + Skills in signal detection, risk assessment, and safety data analysis + Proficiency with safety… more
    Sumitomo Pharma (10/30/25)
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  • Director, Study Responsible Physician - Mivexian

    J&J Family of Companies (Raritan, NJ)
    …also includes individuals from project management , operations, regulatory affairs, data management , medical writing, biostatistics, benefit- risk ... from project management , operations, regulatory affairs, data management , medical writing, biostatistics, drug safety and benefit- risk management… more
    J&J Family of Companies (10/23/25)
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  • Clinical Study Physician

    Teva Pharmaceuticals (Parsippany, NJ)
    …working closely with Disease Area Head, Clinical Development Lead, Clinical Scientist . and other functional areas such as GCO, biostats, regulatory, ... medical accountability and oversight for one or more clinical trials + Matrix management responsibilities across the internal and external network + Manages Phase 1… more
    Teva Pharmaceuticals (10/07/25)
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  • Sr. Medical Director, Clinical Development

    Taiho Oncology (Princeton, NJ)
    …sites regarding a patient's eligibility, dose adjustments, and patient's discontinuation. + Perform data review supported by the CRS on an ongoing basis. Review of ... the safety data will be done through data listings...studies within each of the development programs + Keeps management current on status of both clinical trials and… more
    Taiho Oncology (11/13/25)
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  • Sr. Clinical Trial Physician, Neuroscience

    Bristol Myers Squibb (Madison, NJ)
    …of medical accountability and oversight for multiple clinical trials + Matrix management responsibilities across the internal and external network + Manages Phase 1 ... and may be a member of the Clinical Development Team (CDT) + Leads medical data review of trial data , including eligibility review + Holds responsibility for… more
    Bristol Myers Squibb (10/29/25)
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  • Director, Early Clinical Development - Immunology…

    Bristol Myers Squibb (Madison, NJ)
    … Scientist for medical questions and education (including safety management guidelines) + Assesses key safety-related serious adverse events in partnership ... scientific expertise to cross-functional BMS colleagues + Maintains matrix management responsibilities across internal and external networks **Position Responsibilities**… more
    Bristol Myers Squibb (10/18/25)
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