• Director, Clinical Development

    J&J Family of Companies (Titusville, NJ)
    …Mindset, Drug Discovery Development, Industry Analysis, Innovation, Market Research, Regulatory Affairs Management, Research Ethics, Scientific Evaluation, ... and interpret clinical trial data, provide input into clinical study and regulatory communications and reports, and contribute to clinical development plans and… more
    J&J Family of Companies (11/07/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Trenton, NJ)
    …ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + ... and ensure final transfer of TMF is sufficient to support any potential regulatory filings. + Champion best practices for building and maintaining TMF health.… more
    Sumitomo Pharma (11/05/25)
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  • Manager, Medical Core Content - Neph & Immuno-2

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …product strategy and scientific messaging. + Collaborate cross-functionally with Medical Affairs , Regulatory , Legal, and Commercial teams to ensure consistency ... Collaboration** + Act as key support resource for the Field Medical Affairs team, managing the content repository and version control for field-facing materials… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • J&J Quality & Compliance Internship - Summer

    J&J Family of Companies (Raritan, NJ)
    …master's degree, or PhD in life science, analytical science, data science, regulatory compliance or regulatory affairs , computer science, mathematics, ... with any statistical analysis tools + Awareness of quality management systems or regulatory requirements **FOR US ONLY:** Applicable pay range: $23 per hour to… more
    J&J Family of Companies (11/25/25)
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  • Director, Digital Brand Activation

    Merck (Rahway, NJ)
    …marketing teams within the organization along with sales, product development, regulatory affairs , customer service, and other cross-functional teams to ... of people management experience required + Strong understanding of regulatory requirements and challenges in marketing pharmaceuticals **Required Skills/Abilities:**… more
    Merck (11/24/25)
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  • Senior Principal Scientist, Clinical Research,…

    Merck (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Director May Be… more
    Merck (11/22/25)
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  • Supply Chain Planner

    Heritage Pharma Labs Inc.d/b/a Avet Pharmaceuticals Inc. (East Brunswick, NJ)
    …and inventory levels. + Collaborate with cross-functional teams, (Production, Quality, Regulatory Affairs , Procurement, Sales & Marketing) to align supply ... and support business continuity planning. + Ensure compliance with regulatory and quality requirements specific to the pharmaceutical industry. Specialized… more
    Heritage Pharma Labs Inc.d/b/a Avet Pharmaceuticals Inc. (11/14/25)
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  • VP, Deputy General Counsel, International

    Integra LifeSciences (Princeton, NJ)
    …intercompany loans ; + Providing product counseling and guidance on commercial and regulatory affairs initiatives to ensure compliance with applicable laws and ... in multiple jurisdictions and under a variety of complex legal and regulatory schemes; + Collaborating with the compliance team to ensure Integra's business,… more
    Integra LifeSciences (10/30/25)
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  • Senior Director, Clinical Research,…

    Merck (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more
    Merck (11/22/25)
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  • Principal Scientist, Clinical Research, Immunology

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… more
    Merck (11/22/25)
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