• Associate Director , Medical Affairs…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …through commercial launch-ensuring all products meet rigorous safety, efficacy, and regulatory standards. + Clinical Risk Assessment: Collaborate with the Global ... Investigator-Initiated Studies and Collaborative Research initiatives. + Content Excellence: Review educational, promotional, and advertising materials to ensure clinical… more
    BD (Becton, Dickinson and Company) (06/29/25)
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  • Director of Engineering and Application…

    Citigroup (Rutherford, NJ)
    …the Consent Order Data Use Case Plan, requiring strict adherence to regulatory requirements and enterprise data governance frameworks. Key Responsibilities: + Lead a ... building solutions that prioritize data quality, consistency, and compliance with regulatory requirements. + Provide technical leadership and guidance to development… more
    Citigroup (06/19/25)
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  • Associate Director , Corporate Counsel

    Amneal Pharmaceuticals (Bridgewater, NJ)
    …The incumbent will serve as a member of Amneal's promotional assets review committee (PARC), draft/ review /negotiate general commercial and other types of ... products and actively represent Legal on the company PARC to review promotional/non-promotional materials and strategies covering multiple topics (disease awareness,… more
    Amneal Pharmaceuticals (07/30/25)
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  • VP & Medical Director

    Travelers Insurance Company (Trenton, NJ)
    …which can impact claim outcomes. Organize and coordinate Travelers' medical review functions. This includes interpreting Federal and State regulations and medical ... guidelines to establish medical review policies. Works in close collaboration with the Claim...management, policies and procedures and response to legislative and regulatory issues. + Conduct industry research and analysis related… more
    Travelers Insurance Company (07/25/25)
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  • Head of CCAR Internal Controls - Executive…

    SMBC (Jersey City, NJ)
    …Analysis and Review (CCAR), are robust, effective, and compliant with regulatory requirements. This role is crucial for maintaining the integrity and reliability ... effectiveness of internal controls related to CCAR. + Ensuring compliance with regulatory expectations and internal policies related to CCAR - Collaborating with… more
    SMBC (08/13/25)
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  • Director / Lead Business Development

    Dr. Reddy's Laboratories (Princeton, NJ)
    …sites, prepare diligence reports summarizing findings from the diligence process, review and revise key assumptions following due diligence findings, and update ... Deep understanding of the pharmaceutical industry, including drug development, regulatory pathways, and commercialization strategies. Experience in the generic… more
    Dr. Reddy's Laboratories (08/03/25)
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  • Director of Clinical Research Consulting

    Vitalief (New Brunswick, NJ)
    …for Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials; Regulatory work for start-up document; Contract review and negotiation; ... Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials); Regulatory work required for start-up documents; Processes related to study… more
    Vitalief (07/31/25)
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  • Director / Lead Pricing and Contracting…

    Dr. Reddy's Laboratories (Princeton, NJ)
    …for launches and in-line products. + Lead the pricing committee to establish, review and manage the price approval process. + Conduct financial analysis and develop ... content to support the contract review and approval processes including partnership with legal, market...and approval process working closely with government pricing and regulatory teams. + Work closely with the finance team… more
    Dr. Reddy's Laboratories (08/11/25)
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  • Associate Director Quality Assurance…

    BeOne Medicines (Pennington, NJ)
    …of discrepancies, errors, complaints, failures, or adverse events requiring documented review and action. + Participation in regulatory and customer ... and vendor qualification. + Development of all necessary SOPs, ensuring regulatory compliance in conjunction with being appropriate both clinical and commercial… more
    BeOne Medicines (08/08/25)
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  • Team Lead Model Validation - Executive…

    SMBC (Jersey City, NJ)
    …framework for the Combined US Operations of SMFG by performing independent validation and review of Credit Risk and Stress Testing Models. **SCOPE** As part of the ... and robustness of model ongoing monitoring. + Conducts thorough review on model annual assessment, model changes, and ongoing...large and complex data sets. + Ability to apply regulatory requirements outlined in CECL, IFRS9, SR11-7, capital, CCRA,… more
    SMBC (08/08/25)
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