• Sr Scientist , Regulatory

    Kelly Services (Clark, NJ)
    …individuals in the marketplace. We are proud to offer an opportunity to work as a ** Sr Scientist , Regulatory Affairs ** located in Clark, NJ. **Duration** ... **Compensation** : $50-60/hr **Purpose of the Role: ** 1. Administer regulatory affairs over the product lifecycle from pre-market concept, product development,… more
    Kelly Services (10/26/24)
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  • Sr . Manager, Clinical Scientist

    Pfizer (New York, NY)
    **ROLE SUMMARY** The Clinical Scientist (CS) - Sr . Manager will support clinical epidemiology study execution for multiple studies for one or more vaccine ... programs. In collaboration with Scientific Affairs (SA) / Clinical Epidemiology, Biostatistics group and Clinical Affairs (CA) Operations, the CS is responsible… more
    Pfizer (10/24/24)
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  • Principal Scientist / Director, Global…

    Merck (Rahway, NJ)
    …implementation of internal regulatory strategies and provides mentoring and coaching to Sr . Scientist and Assoc Principal scientist in support of their ... product withdrawal. + Support new technology development. + Demonstrate an understanding of regulatory affairs and applies this understanding to the benefit of… more
    Merck (09/28/24)
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  • Senior Principal Scientist

    Merck (Rahway, NJ)
    …with talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Sr . Principal Scientist ) has primary responsibility ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
    Merck (10/23/24)
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  • Director, Principal Scientist Device…

    Merck (Rahway, NJ)
    …Description of Position-** This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). ... **Job Description** **Position Title** -Director/ Principal Scientist , Regulatory Compliance **Department** - Device...final guidance and standards. + Provide strategic advice to senior management on CMC regulatory matters based… more
    Merck (10/25/24)
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  • Sr . Director, Oncology Asset Development…

    Merck (Rahway, NJ)
    …with talented and dedicated colleagues while developing and expanding your career. The Senior Clinical Director ( Sr . Principal Scientist ) has primary ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
    Merck (10/18/24)
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  • Senior Clinical Director, Immunology

    Merck (Rahway, NJ)
    **Job Description** The ** Senior Clinical Director ( Sr . Principal Scientist )** has primary responsibility for the strategic planning and directing clinical ... Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
    Merck (10/02/24)
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  • Senior Policy Advisor, Bureau of Hepatitis,…

    City of New York (New York, NY)
    …where they are from or where they live. Position Summary: BHHS's Policy and External Affairs Program seeks a Senior Policy Advisor to lead its health systems ... and Treatment, HIV Epidemiology, HIV Prevention, Policy and External Affairs , Racial Equity and Social Justice Initiatives, STI, and...STI, and viral hepatitis policy advocacy more broadly. The Senior Policy Advisor will report to the Director of… more
    City of New York (08/17/24)
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  • Senior Director, Global HTA Value…

    Pfizer (New York, NY)
    …as a regular part of the role responsibilities are GASP, Statistician, Scientific Affairs , Medical Affairs , POL, Clinical Scientist . **RESOURCES MANAGED** + ... **ROLE SUMMARY** The ** Senior Director, HTA, Value & Evidence (HV&E) Medical...reimbursement, and appropriate patient access with global payer and regulatory decision makers. + Partner with internal stakeholders to… more
    Pfizer (10/21/24)
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  • International Medical Director

    Novo Nordisk (Plainsboro, NJ)
    …the Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and ... with, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive the timely… more
    Novo Nordisk (10/17/24)
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  • Director - Safety Surveillance

    Novo Nordisk (Plainsboro, NJ)
    …Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs , Data Management, Biostatistics, Non-clinical, Medical ... safety surveillance sub-function within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and Senior Global Safety… more
    Novo Nordisk (09/13/24)
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