• Sr Principal Product Manager/Strategy

    Oracle (Harrisburg, PA)
    …deep understanding of market trends, customer requirements, competitive landscape, and regulatory changes impacting the higher education sector. + Gather and analyze ... customers, prospects, and partners, with emphasis on registrar's office, academic affairs , and enrollment operations. + Support creation and prioritization of… more
    Oracle (12/12/25)
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  • Director, Global Regulatory Leader

    J&J Family of Companies (Spring House, PA)
    …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory ... candidates from any location to apply. The Director, Global Regulatory Leader in Global Regulatory Affairs...therapy products supporting programs in the Immunology Therapeutic Area. Principal Responsibilities: + As the global regulatory more
    J&J Family of Companies (12/25/25)
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  • Manager, Regulatory Scientist (1 of 3)

    J&J Family of Companies (Titusville, NJ)
    …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory ... Leader (NARL)/Global Regulatory Leader (GRL) for regulatory activities. Principal Responsibilities: + Lead and/or...preferred. + A minimum of 4 years of relevant Regulatory Affairs experience in pharmaceutical, biotech or… more
    J&J Family of Companies (12/25/25)
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  • Senior Regulatory Compliance Coordinator…

    Mount Sinai Health System (New York, NY)
    …or health care policy. + A minimum of 5 years of research experience in Regulatory Affairs , Clinical Affairs or Quality Assurance with knowledge of Phase ... for IRB annual renewal review and approval. + Collaborates with the Principal Investigator (PI) in completion of required regulatory documents including,… more
    Mount Sinai Health System (01/06/26)
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  • Global Regulatory Specialist

    Kelly Services (Philadelphia, PA)
    regulatory documentation to support Management of Change projects. Situated in Global Regulatory Affairs , the specialist will prepare, review and finalize all ... and consistency across multiple systems. This position offers the opportunity for a regulatory affairs professional to further develop a career in the regulation… more
    Kelly Services (12/23/25)
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  • Regulatory Compliance Coordinator - Tisch…

    Mount Sinai Health System (New York, NY)
    …science or legal/ regulatory studies + 3+ years of direct experience in Regulatory Affairs , Clinical Affairs or Quality Assurance within the Medical ... **Job Description** A Regulatory Compliance Coordinator position is currently available within...for IRB review and approval. + Collaborates with the Principal Investigator (PI) in completion of application documents including… more
    Mount Sinai Health System (12/13/25)
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  • Clinical Research Regulatory Coordinator

    Rush University Medical Center (Chicago, IL)
    …(SOPs) are implemented and documented in accordance with study sponsor, Principal Investigator, and regulatory agency specifications. * May collaborate ... on the circumstances of each case. **Summary:** This positions provides regulatory support for multiple clinical research studies, which may involve multi-centered… more
    Rush University Medical Center (11/26/25)
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  • Regulatory Coordinator

    Georgetown Univerisity (Washington, DC)
    …life science, or related field + Minimum of 2 years of experience in regulatory affairs or clinical research + FDA, ICH-GCP) Familiarity with regulatory ... dedication to making a difference in the world. Requirements Job Overview The Regulatory Coordinator plays a critical role in ensuring regulatory compliance and… more
    Georgetown Univerisity (11/21/25)
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  • Regulatory Specialist (Hybrid Opportunity)

    Stanford University (Stanford, CA)
    …including project management in a dynamic research setting. + Strong knowledge of regulatory affairs , including FDA regulations, IRB review and approval process, ... scientific area between the investigators and regulatory agencies. Provide regulatory support, guidance, and information to principal investigators and… more
    Stanford University (11/20/25)
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  • Lead SaMD Technical Program Manager

    Wolters Kluwer (Chicago, IL)
    Principal SaMD TPM acts as a bridge between engineering, product, regulatory affairs , clinical, and quality assurance teams, facilitating strategic ... The ** Principal SaMD Technical Program Manager** plays a pivotal...**Cross-Functional Collaboration:** Act as a liaison between engineering, product, regulatory affairs , clinical, and QA teams to… more
    Wolters Kluwer (12/04/25)
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