• Senior Specialist, Project Management - Chemistry…

    Merck (Rahway, NJ)
    …n/a **Required Skills:** Adaptability, Change Management, Clinical Supplies Management, Clinical Supply Chain Management, Clinical Trial Management, ... holistic portfolio management and increased integration of CMC and Clinical strategies. **Position Description/Summary:** The CIPM Senior Specialist, Project… more
    Merck (08/28/25)
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  • Senior Specialist, Project Management - Drug…

    Merck (Rahway, NJ)
    …Adaptability, Business Management, Change Management, Clinical Supplies Management, Clinical Supply Chain Management, Clinical Trial Management, ... includes integrating strategic and tactical input from diverse disciplines (eg, clinical , regulatory, market access, manufacturing, CMC, commercial, and other areas)… more
    Merck (08/27/25)
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  • Manager, eCOA Management

    Bristol Myers Squibb (Madison, NJ)
    …understanding of drug development, eCOA and UAT processes. + Solid experience with clinical trial solutions, specifically with eCOA instruments and with testing ... is essential to the study level operationalization of the eCOA capability for BMS clinical trials and directly contributes to the BMS R&D pipeline. This role reports… more
    Bristol Myers Squibb (07/27/25)
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  • Senior Director, Communications,…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …and competitors as well as a general understanding of important topics including clinical trial design, drug development, regulatory decision making and public ... communications advisor to leaders in Commercial and Brand, Medical Affairs, Clinical Development and Portfolio Strategy regarding strategic TA, product and pipeline… more
    Otsuka America Pharmaceutical Inc. (07/26/25)
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  • Full Time Home Infusion Nurse

    Naven Health (Hamilton, NJ)
    …infusion services for a broad range of specialized therapies, as well as clinical trial services and special programs for pharmaceutical manufacturers. Joining ... always.** Naven Health is a nationwide home infusion nursing network and clinical platform focused on delivering specialized, truly exceptional infusion care. With… more
    Naven Health (08/28/25)
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  • Senior Principle Scientist, Regulatory Liaison…

    Merck (Trenton, NJ)
    …+ Conduct initial content review and approval for IND/CSA submissions to enable clinical trial initiation. + Participate in regulatory due diligence activities ... final regulatory review and approval of: + Worldwide marketing applications + Clinical study protocols and reports + Investigator brochures + Local registration… more
    Merck (08/23/25)
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  • Director, Biologics Process Development (BPD)

    Merck (Rahway, NJ)
    …not limited to Investigational New Drugs, Investigational Medicinal Product Dossiers, and Clinical Trial Applications. + Ability to work closely with ... high yields along with superior product quality and allow speedy progression for clinical studies and commercial launch. The candidate will be a member of the… more
    Merck (08/20/25)
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  • Senior Director, CNS Communications

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …and competitors as well as a general understanding of important topics including clinical trial design, drug development, regulatory decision making and public ... communications advisor to leaders in Commercial and Brand, Medical Affairs, Clinical Development and Portfolio Strategy regarding strategic TA, product and pipeline… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Director, Statistical Innovation (Office-based)

    AbbVie (Florham Park, NJ)
    …Leverage state of art modeling and simulation techniques to propose, evaluate and optimize clinical trial designs in terms of time, cost and probability of ... quantitative consulting/simulations to solve complex and non-standard problems in clinical development​. The Director, Statistical Innovation is responsible for… more
    AbbVie (08/08/25)
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  • Principal Statistical Programmer

    Regeneron Pharmaceuticals (Warren, NJ)
    …or related discipline with 3+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related ... provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis… more
    Regeneron Pharmaceuticals (07/31/25)
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