• Global Commercial Lead, AskBio-1005, Parkinson's…

    Bayer (Cambridge, MA)
    …the Regenerative Medicine Advanced Therapy (RMAT) designation by the US Food & Drug Administration ( FDA ) to slow disease progression and improve motor ... outcomes in patients with PD. A randomized, double-blinded study is currently being conducted in the US, EU and UK. Successful commercialization of this asset provides an exciting challenge as we enter this new and important therapeutic area, The cell therapy… more
    Bayer (08/27/25)
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  • Clinical Trials Manager, Clinical…

    Gilead Sciences, Inc. (Foster City, CA)
    …effectively articulates and interprets these. + Thorough knowledge of Food & Drug Administration ( FDA ), European Medicines Agency (EMA), and other ... applicable national regulations, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) governing the conduct of clinical studies. + Familiar with standard medical /… more
    Gilead Sciences, Inc. (08/21/25)
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  • Clinical Trials Manager

    Gilead Sciences, Inc. (Foster City, CA)
    …workload based upon changing priorities + Complete knowledge of Food & Drug Administration ( FDA ), European Medicines Agency (EMA), and other applicable ... national regulations, International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, Good Clinical Practice (GCP) and key Clinical Operations principles, concepts, practices, standards, processes and… more
    Gilead Sciences, Inc. (08/13/25)
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  • Research Analyst I - Immunotox

    Charles River Laboratories (Mattawan, MI)
    …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on… more
    Charles River Laboratories (09/04/25)
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  • Sr. Global Operational Excellence Manager

    Balchem (Montvale, NJ)
    …Protection Agency (EPA), Equal Employment Opportunity (EEO), and Federal Food and Drug Administration ( FDA ) regulations. + Ability and willingness to ... This position is responsible for leading process performance improvements in a food manufacturing environment (The specific activities are listed in the Essential… more
    Balchem (07/10/25)
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  • Inpatient Clinical Pharmacist III, Transitions…

    Sutter Health (Sacramento, CA)
    …Security (DHS), Drug Enforcement Administration (DEA), Food and Drug Administration ( FDA ) and United States Pharmacopeia (USP). + Possess written ... glad you are interested in joining Sutter Health! **Organization:** SMCS-Valley Administration **Position Overview:** Transitions of Care management - focused on… more
    Sutter Health (08/30/25)
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  • Functional Software Project Manager

    General Dynamics Information Technology (Silver Spring, MD)
    …communication skills that is interested in becoming part of our ** Food and Drug Administration ( FDA )** team, supporting our customers with their critical ... Prior or current experience working in a similar role at the Food and Drug Administration + Appian technology experience \#GDITFedHealthJobs The likely… more
    General Dynamics Information Technology (09/12/25)
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  • Quality Assurance Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …thorough understanding of the following regulations and guidelines: US Food and Drug Administration ( FDA ) regulations, ISO 9001, ISO 13485, Medical ... distribution of medical products is in compliance with corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical… more
    Integra LifeSciences (08/17/25)
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  • Center Medical Director (CMD)

    CSL Plasma (Indianapolis, IN)
    …primary center physician registered as the Laboratory Director with the Food and Drug Administration ( FDA ). **Job Description** + Serves as the primary ... physician for reporting to the Food and Drug Administration and in such capacity provides medical oversight in compliance with applicable Federal and State… more
    CSL Plasma (07/03/25)
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  • Research Analyst I- Bioanalytical

    Charles River Laboratories (Cleveland, OH)
    …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and… more
    Charles River Laboratories (09/03/25)
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