• Principal Scientist , Upstream Process R&D

    Merck (Rahway, NJ)
    …to join Biologics Process Research & Development (BPR&D) as a Principal Scientist . BPR&D within Research Laboratories is on a mission to rapidly deliver ... To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing… more
    Merck (08/20/25)
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  • Senior Director, Clinical Research,…

    Merck (Rahway, NJ)
    **Job Description** The Senior Director ( Sr . Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
    Merck (09/04/25)
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  • Clinical Trial Physician/ Senior

    Bristol Myers Squibb (Madison, NJ)
    …eligibility review + Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including ... strategic oversight in protocol development (input on inclusion/exclusion and other safety -related clinical considerations) + Fulfills GCP and compliance… more
    Bristol Myers Squibb (08/25/25)
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  • Senior Medical Director, Oncology Asset…

    Merck (Rahway, NJ)
    …dedicated colleagues while developing and expanding your career. The Senior Clinical Director ( Sr . Principal Scientist ) has primary responsibility for ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
    Merck (08/20/25)
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  • Senior Director, Immunology…

    Bristol Myers Squibb (Madison, NJ)
    …years required clinical trial experience in pharmaceutical industry setting (eg, Clinical Trial Physician, Clinical Scientist ); expertise in drug ... protocol and ICF, providing medical input during protocol development to ensure clinical relevance, scientific rigor, patient safety , and alignment with study… more
    Bristol Myers Squibb (09/04/25)
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  • Director, Early Clinical Development…

    Bristol Myers Squibb (Madison, NJ)
    …lifecycle + Manages site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines) ... strategic oversight in protocol development (input on inclusion/exclusion and other safety -related clinical considerations) + Fulfills GCP and compliance… more
    Bristol Myers Squibb (08/12/25)
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  • Imaging Lead

    Merck (Trenton, NJ)
    **Job Description** **Brief Description** **of** **Position** The Imaging Lead ( Sr . Principal Scientist ) works with Clinical Imaging Scientists to support ... use of imaging, and oversees the work of the Clinical Imaging Scientist to ensure that timelines...preferred. + Knowledge of the use of imaging in clinical trials for evaluation of efficacy and safety more
    Merck (08/19/25)
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  • Global Project Head, Rare

    Sanofi Group (Morristown, NJ)
    …dotted-line management toward all GPT members, including eg project management, clinical operations, regulatory, safety , translational medicine, statistics, CMC, ... Project Head (GPH) is delegated various responsibilities by the Senior GPH and/orTherapeutic Area Head to provide leadership, supervision,...IA **Basic Qualifications:** + Medical doctor or doctor/ scientist + More than 5 years of … more
    Sanofi Group (07/30/25)
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  • Principal Sterilization Microbiologist

    System One (Park Ridge, NJ)
    …hands-on testing when necessary. Your expertise will directly impact product safety , regulatory success, and speed-to-market for critical medical devices and ... strategies aligned with corporate innovation and compliance goals. The Principal Scientist must demonstrate a high level of autonomy, demonstrating ownership,… more
    System One (06/26/25)
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