• Senior Principal Scientist

    Merck (Rahway, NJ)
    …interaction with key scientific leaders. **Specifically, the Senior Principal Scientist is responsible for:** + Planning clinical trials (design, operational ... timely and equitable access to our medicines. The Senior Principal Scientist has primary responsibility for protocol...will apply an in-depth understanding of HIV and drug pharmacology to the infectious disease therapeutic area's clinical more
    Merck (11/22/25)
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  • Senior Principal Scientist

    Merck (Rahway, NJ)
    **Job Description** **Senior Principal Scientist Translational Medicine, Immunology** Translational Medicine in our Research & Development Division is ... clinical Proof-of-Concept (Phase 2a), and development and execution of clinical pharmacology strategies for late-stage development programs from… more
    Merck (11/26/25)
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  • Principal Scientist Transporters

    Bristol Myers Squibb (Princeton, NJ)
    …Myers Squibb Drug Metabolism and Pharmacokinetics (DMPK) Department seeks a passionate Principal Scientist to provide scientific leadership and mentorship within ... vivo transporter assessments; applying mechanism-based approaches to the quantitative translation of pre- clinical in vitro and in vivo data to clinical findings.… more
    Bristol Myers Squibb (11/28/25)
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  • Senior Clinical Trial Physician,…

    Bristol Myers Squibb (Madison, NJ)
    …review * Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety ... and upper management of key functions (eg, early development, TM, clinical pharmacology , toxicology, regulatory, HEOR, market access, medical affairs),… more
    Bristol Myers Squibb (11/22/25)
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  • Director, Early Clinical Development (MD)…

    Bristol Myers Squibb (Madison, NJ)
    clinical lifecycle + Manages site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety ... Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and...proof of concept Phase I/II, entry registrational studies, and/or clinical pharmacology studies + Liaises with … more
    Bristol Myers Squibb (11/21/25)
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