• Director, Integrated Publications

    Taiho Oncology (Princeton, NJ)
    …plan for scientific and clinical studies in process, prior to regulatory submissions, and assessment of secondary publication plan development and alignment ... unmet needs for informing the publications strategy. Education/Certification Requirements: PhD /PharmD with minimum 8-10 years combined experience in the… more
    Taiho Oncology (07/25/25)
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  • Product Advisor III - International Treasury

    PNC (East Brunswick, NJ)
    …/ college degree. Higher level education such as a Masters degree, PhD , or certifications is desirable. Industry relevant experience is typically 8+ years. ... Mortgage Licensing Act of 2008 (SAFE Act) and/or the Financial Industry Regulatory Authority (FINRA), which prohibit the hiring of individuals with certain criminal… more
    PNC (07/25/25)
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  • Field Director, Medical Science Liaison…

    Grifols Shared Services North America, Inc (Atlantic City, NJ)
    …exceed goals and objectives. + Ensures compliance with all applicable regulatory , legal, and operational rules and procedures of their team. ... background with advanced degree in a scientific field of study (PharmD, MD, PhD , or advanced/Master's nursing degree) + Typically requires 4 or more years of… more
    Grifols Shared Services North America, Inc (07/24/25)
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  • Senior Medical Science Liaison - Biopharma…

    Sumitomo Pharma (Jersey City, NJ)
    …Health preferred. + Advanced degree in medical science (MD, PharmD, or PhD ) is strongly preferred. Candidates without an advanced degree are required to ... confidential. **Compliance** : Achieve and maintain Compliance with all applicable regulatory , legal and operational rules and procedures, by ensuring that all… more
    Sumitomo Pharma (07/23/25)
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  • R&D Microbiology Manager- Foods

    Unilever (Englewood Cliffs, NJ)
    …- Representing and guiding Unilever as the face of Microbiology to external regulatory bodies (FDA, CFIA, etc.) + Micro validation support (formulation advice to ... in Food Microbiology with 5 - 7 years related experience, or preferred PhD degree in Microbiology with minimum 1-2 years post-graduate experience, or a Bachelor… more
    Unilever (07/19/25)
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  • Senior Relationship Strategist - PNC Private Bank

    PNC (Ridgewood, NJ)
    …/ college degree. Higher level education such as a Masters degree, PhD , or certifications is desirable. Industry relevant experience is typically 8+ years. ... Mortgage Licensing Act of 2008 (SAFE Act) and/or the Financial Industry Regulatory Authority (FINRA), which prohibit the hiring of individuals with certain criminal… more
    PNC (07/16/25)
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  • Executive Director, CNS Strategy, Global Medical…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …and advocates for Otsuka prominence in CNS space + Provides input into regulatory documents, including product labeling + Accountable for resourcing of personnel and ... + Ensures development and growth of team members **Qualifications:** + MD, DO, PhD , PharmD or equivalent advanced degree is required + Strong CNS understanding and… more
    Otsuka America Pharmaceutical Inc. (07/11/25)
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  • Manager, Embedded Software V&V

    Ford Motor Company (Trenton, NJ)
    …+ Ensure all V&V activities comply with relevant industry standards, regulatory requirements, and internal quality processes (eg, functional safety standards, ... teams and stakeholders. Even better, you may have + Master's or PhD degree in a relevant engineering field. + Experience with safety-critical embedded… more
    Ford Motor Company (07/11/25)
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  • Associate Director, Promotional Materials

    Taiho Oncology (Princeton, NJ)
    …teams regarding communications strategy and planning. + Review and approve the regulatory content of materials created for product promotion, corporate, and other ... Requirements: + Advanced degree in life or health sciences (Pharm.D., PhD , MS) and/or healthcare professional license with significant experience in review… more
    Taiho Oncology (07/04/25)
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  • Associate Statistical Project Leader

    Sanofi Group (Morristown, NJ)
    …and scientific validity of the content according to internal standards and regulatory guidelines and in compliance with SOPs. + Propose, prepare and perform ... ad-hoc analyses as relevant for the study or project objectives. **About You** + PhD /MS in statistics or related discipline with at least 3 years of pharmaceutical… more
    Sanofi Group (07/03/25)
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