• Director/Principal Scientist, Regulatory

    Merck (Rahway, NJ)
    **Job Description** At the heart of innovation, our Regulatory Affairs team plays a vital role in delivering new medical advancements to patients around the ... regulatory strategy and submissions through collaboration with Regulatory Affairs Europe (RAE) and local affiliate...content review and approval for IND/CSA submissions to enable clinical trial initiation. + Participate in regulatory more
    Merck (08/02/25)
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  • Regulatory Affairs Process…

    Kelly Services (Sunnyvale, CA)
    Kelly(R) Science & Clinical is seeking a Regulatory Affairs Process Specialist for a 6-month contract opportunity with a leading molecular diagnostics ... & Clinical **Overview and Responsibilities** + The Regulatory Affairs Process Specialist will work with...of future opportunities in the field of science and clinical research . \#P1 As part of our… more
    Kelly Services (07/24/25)
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  • Regulatory Affairs Principal, NPD

    Kelly Services (Sunnyvale, CA)
    **Kelly(R) Science & Clinical ** is currently recruiting a ** Regulatory Affairs Principal** for an **12-month contract** opportunity with a leading molecular ... Product Development **Pay rate:** $60-63/hour **Company:** Kelly(R) Science & Clinical **Overview:** The Regulatory Affairs ...of future opportunities in the field of science and clinical research . \#P1 As part of our… more
    Kelly Services (07/18/25)
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  • RayzeBio Director, Medical Affairs

    Bristol Myers Squibb (San Diego, CA)
    …of study-related information. This role will work cross-functionally with several departments ( Clinical Operations, CMC, Regulatory Affairs , Supply Chain, ... the global leader in radiopharmaceuticals . The Director, Medical Affairs Research Operations, plays an integral role...both within medical affairs as well as clinical development, clinical operations, regulatory ,… more
    Bristol Myers Squibb (07/25/25)
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  • Regulatory Affairs Specialist 4

    Hologic (Newark, DE)
    …various functions across the business, including but not limited to Regulatory Affairs , Research and Development, Clinical , Quality, and Marketing. Works ... Regulatory Affairs Specialist 4 Newark, DE,...annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and… more
    Hologic (07/12/25)
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  • Regulatory Affairs Project Manager

    Abbott (Sylmar, CA)
    regulatory guidelines, policies and regulations + Ethical guidelines of the regulatory profession, clinical research and regulatory process ... experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs , operations, or related area.… more
    Abbott (05/08/25)
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  • Associate Director Regulatory

    Abbott (San Diego, CA)
    …international regulatory guidelines, policies and regulations Ethical guidelines of the regulatory profession, clinical research and regulatory ... experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs , operations, or related area. +… more
    Abbott (07/10/25)
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  • Director, CMC Regulatory Affairs

    Gilead Sciences, Inc. (Foster City, CA)
    …submission and approval process in close partnership with other functions in PDM, Regulatory Affairs , and Clinical Development. + Responsible for development ... and serious respiratory and cardiovascular conditions. **KEY RESPONSIBILITIES** The Director, CMC Regulatory Affairs for Biologics is responsible for defining … more
    Gilead Sciences, Inc. (08/02/25)
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  • Senior Regulatory Affairs Specialist…

    Abbott (Santa Clara, CA)
    …experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs , operations, or related area. + ... software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an onsite... review. + Monitor and submit applicable reports to regulatory authorities. + Evaluate proposed preclinical, clinical more
    Abbott (07/29/25)
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  • Associate Director, Search & Evaluation

    AbbVie (Cambridge, MA)
    …one aspect of Drug Development (eg, pre- clinical research , clinical development, Regulatory Affairs , Chemistry Manufacturing and Controls (CMC)). ... Include: + Proactively search for, identify, and evaluate potential opportunities ( research collaboration, in-licensing preclinical and clinical assets, platform… more
    AbbVie (05/28/25)
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