• Director, Global Strategic Marketing, Tri-Specific…

    J&J Family of Companies (Raritan, NJ)
    …strategies, tactics, customer solutions and messaging. + Work closely with Medical Affairs to ensure robust publication plans and enduring/differentiating ... to understand, interpret and communicate commercial and competitive implications of technical/clinical/ regulatory data . This individual has the capability to… more
    J&J Family of Companies (09/06/25)
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  • Senior Director of Global Marketing, Growth…

    Ascendis Pharma (Princeton, NJ)
    …International marketing and business leads and other cross-functional teams, including R&D, regulatory , medical affairs , and regional commercial teams, to ... plan. + Update Skytrofa core claims in line with significant publications and data releases; ensure expectations on in-market implementation are met. + Maintain the… more
    Ascendis Pharma (09/01/25)
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  • Director, Sustainability Enablement

    Bristol Myers Squibb (Madison, NJ)
    …will act as a pivotal resource for technical, operational, and regulatory expertise, driving sustainable practices across the organization. **Key Responsibilities** ... development of a robust scope 3 roadmap to achieve Net Zero, including data collection, analysis, and reduction strategies for indirect emissions across the value… more
    Bristol Myers Squibb (09/05/25)
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  • Senior Fraud/AML Investigator

    Guardian Life (Holmdel, NJ)
    …We drive a high-performance culture across our Legal, Compliance, and Government Affairs functions, aligned to "what" we deliver (ie, our goals and objectives) ... internal and external investigations including interpreting allegations, collecting relevant data in support of fact finding and analysis, conducting detailed… more
    Guardian Life (09/04/25)
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  • Senior Director, MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …appropriate. + Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs , and Operations to align strategies and optimize ... process validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process Verification… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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  • Clinical Documentation Global Head

    Sanofi Group (Morristown, NJ)
    …qualified with: + Min 15 years of experience working in clinical development and/or regulatory affairs + Min 10 years of leading an internationally dispersed ... of sanofi revenues by expediting submission timelines and facilitating reviews by regulatory agencies of sanofi key assets. + He/she: Creates and executes a… more
    Sanofi Group (07/02/25)
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  • Senior Legal Counsel, Digital Partnerships

    CVS Health (Parsippany, NJ)
    …wellness products and services. You will collaborate closely with internal digital, data , analytics, technology, and other business partners to build a useful and ... solutions to balance risks with business objectives. Your expertise in health care, data use, and digital technology will allow you to understand and support the… more
    CVS Health (09/06/25)
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  • Associate Director, Competitive Intelligence-…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …group of therapeutic area partners (including Commercial, Medical Affairs , Affiliates, Clinical, Research, Corporate Development, Regulatory , and Legal) ... Providing conference coverage and analytic support of emerging clinical and market data . + Evaluating and making recommendations on CI tools, processes, and services… more
    Gilead Sciences, Inc. (08/21/25)
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  • Sales Specialist, Diagnostic Oncology (Central…

    Fujifilm (Trenton, NJ)
    …with expense tracking and reporting (Salesforce.com) + Where appropriate, collaborate with the Medical Affairs Team. + Follow up to define pathway and respond ... what is working and not working. + Reviews sales data , assesses trends, and adjusts sales strategy based upon...all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485… more
    Fujifilm (08/14/25)
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  • Manager, R&D Paralegal

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …start-up documents including patient recruitment materials and indemnification letters ** Medical Affairs Paralegal Functions:** + Independently review, revise, ... Key responsibilities will include assisting with contract negotiation and management, legal/ regulatory research, and internal data tracking management. The R&D… more
    Otsuka America Pharmaceutical Inc. (08/08/25)
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