• Regulatory and Safety Affairs

    Reckitt (Parsippany, NJ)
    Regulatory and Safety Affairs Associate City: Parsippany **We are Reckitt** Home to the world's best loved and trusted hygiene, health, and nutrition ... to grow in our great organisation. **About the role** The Regulatory Affairs & Safety Associate , Regulatory and Compliance provides regulatory more
    Reckitt (11/04/25)
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  • Associate Director, Regulatory

    Gilead Sciences, Inc. (Parsippany, NJ)
    …their aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director, Global Regulatory Affairs , you will act as ... role in ad hoc or special projects that continuously improve or otherwise advance Regulatory Affairs capabilities. Position will be filled in either Foster City,… more
    Gilead Sciences, Inc. (10/23/25)
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  • Assoc Director, Medical Affairs

    Gilead Sciences, Inc. (Parsippany, NJ)
    …please visit Gilead.com. We have an exciting opportunity within the US Medical Affairs (USMA) organization for an Associate Director within Oncology Medical ... experience inOncologyMedicalAffairs + Industry experience with knowledge of all applicable regulatory and legal requirements for Medical Affairs activities +… more
    Gilead Sciences, Inc. (11/15/25)
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  • Associate Director, Medical Writing…

    J&J Family of Companies (Raritan, NJ)
    …as Medical Affairs , Medical Safety , Post Market Surveillance, Clinical Affairs , Design Quality Engineers, R&D, and Regulatory Affairs relating to ... at https://www.jnj.com/medtech We are searching for the best talent for an ** Associate Director, Medical Writing & Literature Services** . _Remote work options may… more
    J&J Family of Companies (11/15/25)
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  • Associate Director, Biostatistics

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …study team and key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical operation. + ... products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of...sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Associate Director, ICSR Management Team…

    Ascendis Pharma (Princeton, NJ)
    Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Expert knowledge of FDA safety ... for employees to grow and develop their skills. The Associate Director, ICSR Management Team reports to the Director,... regulatory guidance documents; working knowledge of global safety regulations. + Ability to travel up to 20%… more
    Ascendis Pharma (10/09/25)
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  • Associate Director, Statistics - Immunology

    AbbVie (Florham Park, NJ)
    …of work may include clinical trials, patient safety , and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... and drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety , and GMA, etc.) to create development… more
    AbbVie (10/15/25)
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  • Associate Director, Outcomes Research

    Organon & Co. (Jersey City, NJ)
    **Job Description** **The Position** The role of Associate Director, Dermatology Outcomes Research Epidemiology and Economics will report to the headquarters ... Director of Medical Affairs Outcomes Research. Focusing on Dermatology, in this role, you will be responsible for establishing/continuing economic Modelling research… more
    Organon & Co. (11/04/25)
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  • Associate Director, US Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, US Medical Neuropsychiatry position works in the US Medical ... points across US functional and commercialization areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical Neuropsychiatry.… more
    Bristol Myers Squibb (10/30/25)
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  • Senior Clinical Director, Oncology Early…

    Merck (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Management Process, Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance {+ 5 more}… more
    Merck (11/18/25)
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