• Life Science Associate Director - Strategic…

    Cognizant (Teaneck, NJ)
    …broad life-sciences domain experience * Minimum 10+ years in in experience in clinical trial life-cycle and pharma sponsor and site engagement **Preferred ... **Title: Associate Director , Strategic Product Management (Life Sciences Products &...workshops/digital dialogues/demos/PoCs * Provide input for Pre-Sales team to support priority customers in imagining how solutions can improve… more
    Cognizant (08/20/25)
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  • Director , Biologics Process Development…

    Merck (Rahway, NJ)
    …not limited to Investigational New Drugs, Investigational Medicinal Product Dossiers, and Clinical Trial Applications. + Ability to work closely with ... seeking an experienced leader who will manage a team of scientists to support drug substance process development activities to enable and accelerate early and… more
    Merck (08/20/25)
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  • Principal Scientist, Clinical Research, GI…

    Merck (Rahway, NJ)
    … Sciences, Clinical Testing, Clinical Trial Planning, Clinical Trial Support , Cross-Functional Teamwork, Data Analysis, Hematology, Intellectual ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...or marketed Oncology drugs + Analyzing and summarizing the clinical findings from studies to support decisions… more
    Merck (08/16/25)
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  • Associate Director , Medical Affairs…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …for regulatory submissions and communicate with FDA and international authorities to support safety, efficiency, and clinical performance claims. + Global ... Medical Affairs Support : Ensure comprehensive Medical Affairs support to worldwide Sales and Marketing teams. + Industry...You are an exceptional leader with demonstrated expertise in clinical strategy, trial design, and execution. You'll… more
    BD (Becton, Dickinson and Company) (06/29/25)
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  • Senior Principal Scientist, Clinical

    Merck (Rahway, NJ)
    …external opportunities. + Provide support for other therapeutic areas regarding clinical issues related to Neuroscience. **The Senior Director may:** + ... post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical... Clinical Neurophysiology, Clinical Research Management, Clinical Testing, Clinical Trial Development,… more
    Merck (08/20/25)
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  • SEC Compliance Manager/ Director

    Robert Half Finance & Accounting (Cranbury, NJ)
    …regulations, SOX, and internal policies. + Manage complex transactions including clinical trial accruals, stock-based compensation, revenue recognition, and ... client, a rapidly growing pharmaceutical company, is seeking a Director of SEC Reporting to lead technical accounting operations...of SEC Reporting to lead technical accounting operations and support its path toward a potential IPO. This role… more
    Robert Half Finance & Accounting (07/18/25)
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  • Director , GHEOR Neuroscience

    Bristol Myers Squibb (Princeton, NJ)
    …access strategy, clinical , medical affairs, and commercial. + Give input into clinical trial design and endpoints aligned to value demonstration strategy. + ... and later indications with input from key stakeholders such as Clinical , Medical, Marketing, Market Access, Statistics and Regulatory. **Responsibilities:** + Lead… more
    Bristol Myers Squibb (07/24/25)
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  • Senior Director , US Commercial Asset…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …R&D organizations + Demonstrated knowledge/aptitude in pharmaceutical product development, clinical trial design and research, scientific evidence generation. ... **Position Summary** The Senior Director , US Commercial Asset Planning is responsible for...all stages of their lifecycle receive strategic leadership, commercialization support , and alignment with Otsuka's long-term business objectives. **Key… more
    Otsuka America Pharmaceutical Inc. (08/15/25)
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  • Director /Principal Scientist, Regulatory…

    Merck (Rahway, NJ)
    …+ Conduct initial content review and approval for IND/CSA submissions to enable clinical trial initiation. + Participate in regulatory due diligence activities ... Responsibilities** + Develop and lead global regulatory strategies to support multiple indications, optimizing labels and achieving timely regulatory approvals.… more
    Merck (08/19/25)
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  • Senior Principal Scientist, Clinical

    Merck (Rahway, NJ)
    Clinical Research, Clinical Research Management, Clinical Studies, Clinical Testing, Clinical Trial Development, Clinical Trials, ... medicines. With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical...marketed cardiovascular and respiratory drugs + Analyzing and summarizing clinical findings from studies to support decisions… more
    Merck (08/20/25)
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