• R&D Packaging Engineer, Regional Packaging…

    Reckitt (Evansville, IN)
    …Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a ... we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products...and environments. You will also have access to our Research and Development Academy, designed to develop our team… more
    Reckitt (11/13/25)
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  • Senior Director, Compliance & Ethics, Global R&D

    Teva Pharmaceuticals (Parsippany, NJ)
    …HR, Medical Affairs, Specialty Clinical , + Pre- Clinical /Pharmacology, Regulatory , Pharmacovigilance, Health Economics & Outcomes Research , Generics, and ... have strong healthcare industry knowledge, including knowledge and experience working with Clinical and Pre- Clinical Research , Generics, Medical Affairs,… more
    Teva Pharmaceuticals (09/25/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Columbia, SC)
    …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... in study planning with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on TA… more
    Parexel (10/11/25)
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  • Assoc Director, Biostatistics

    Gilead Sciences, Inc. (Foster City, CA)
    …of assigned studies by collaborating with cross-functional partners to meet clinical development project deliverables and timelines. This may include, ... into clinical development documentation, scientific publications and presentations, and regulatory filings. Dependent upon the area of assignment, you may lead… more
    Gilead Sciences, Inc. (11/13/25)
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  • Sr Manager, Biostatistics

    Gilead Sciences, Inc. (Foster City, CA)
    …of assigned studies by collaborating with cross-functional partners to meet clinical development project deliverables and timelines. This may include, ... into clinical development documentation, scientific publications and presentations, and regulatory filings. Dependent upon the area of assignment, you may lead… more
    Gilead Sciences, Inc. (11/12/25)
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  • Associate Director, Biostatistics

    Gilead Sciences, Inc. (Foster City, CA)
    …of assigned studies by collaborating with cross-functional partners to meet clinical development project deliverables and timelines. This may include, ... into clinical development documentation, scientific publications and presentations, and regulatory filings. Dependent upon the area of assignment, you may lead… more
    Gilead Sciences, Inc. (10/22/25)
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  • TA Head of Biostatistics, Neuroscience…

    Sanofi Group (Cambridge, MA)
    …Ophthalmology TA, from clinical development plan inception to approval by regulatory bodies as applicable, ensuring project teams are provided with strong ... TA Biostatistics.** You will be leading and overseeing all statistical work for clinical development and regulatory submissions, leading a team focused on … more
    Sanofi Group (10/16/25)
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  • Senior Environmental Health, Safety…

    Charles River Laboratories (Hollister, CA)
    …and ensure compliance with regional, state and federal safety and environmental regulatory agencies. + Maintain and ensure timely reporting of safety and ... environmental data, documentation, permits and licenses to all applicable regulatory agencies. Assess new regulatory standards and identify program changes to… more
    Charles River Laboratories (11/07/25)
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  • Senior Director of API Manufacturing

    Kelly Services (South San Francisco, CA)
    …you're connected to a wealth of future opportunities in the field of science and clinical research \#P1 As part of our promise to talent, Kelly supports those ... Director of CMC, you'll be instrumental in overseeing API process scale-up, regulatory strategy, and operational excellence required for clinical and commercial… more
    Kelly Services (09/30/25)
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  • Compliance Senior Specialist and Technical Writer

    Merck (Lower Gwynedd, PA)
    …(eg, neutralization assays) will be utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings. As the AdVAnce ... Information Management System (LIMS), Laboratory Investigations, Process Improvement Projects, Project Management, Regulatory Compliance, Regulatory Strategy… more
    Merck (11/15/25)
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