• Associate Principal Scientist,…

    Merck (West Point, PA)
    …scientist for the Drug Metabolism and Pharmacokinetics (DMPK) group. The Associate Principal Scientist will be a key contributor to multi-disciplinary drug ... the discovery and clinical development of therapeutics across various modalities. The Associate Principal Scientist will guide the design and interpretation of in… more
    Merck (05/17/24)
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  • IIT Program Director

    University of Colorado (Aurora, CO)
    …including but not limited to study workloads and characteristics (multicenter, IND /IDE, etc), opening timelines, and accruals. + Develop internal relationships with ... strategic goals with guidance from the OCRST Program Director and Deputy Associate Director of Clinical Research. + Collaborates with the Data Safety Monitoring… more
    University of Colorado (05/09/24)
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  • Customer Program Manager-Subcomponents (1st shift,…

    Component Repair Technologies (Mentor, OH)
    …OVERVIEW Component Repair Technologies (CRT) is a locally family-owned business, with operations in Mentor, OH since 1985. Our staff of approximately five hundred ... 3. Create technical findings report as to necessary repairs. 4 . Develop and ensure work scopes are communicated to...setting, or relevant industry. 2. A minimum of an associate degree or equivalent work experience. 3. Exposure to… more
    Component Repair Technologies (05/15/24)
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  • Synthetics Principal Product Quality Leader

    Amgen (Thousand Oaks, CA)
    Operations , Scientific, or Manufacturing experience OR + Master's degree & 4 years of Quality, Operations , Scientific, or Manufacturing experience OR + ... Bachelor's degree & 6 years of Quality, Operations , Scientific, or Manufacturing experience OR + Associate...year experience with authoring or review of market applications, IND , supplements or similar regulatory documentation + 1+ year… more
    Amgen (05/13/24)
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  • Regulatory Coordinator

    Beth Israel Lahey Health (Boston, MA)
    …for regulatory findings. Rectifies identified issues and tracks trends and patterns 4 . Maintains and tracks all necessary protocol training for new and current ... May be tasked with assisting in Serious Adverse Event (SAE) reporting, IND submissions and safety reporting, and notification of protocol non-compliance (deviation… more
    Beth Israel Lahey Health (03/31/24)
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  • Director Clinical Development

    Intra-Cellular Therapies, Inc (New York, NY)
    …integrity and respect in all we do, create and deliver. The Associate Director/Director Clinical Development, will be responsible for the leadership, oversight, and ... studies. Develop and maintain relationships with sites and Investigators. 4 . Provide medical monitoring, which includes reviewing study participant eligibility,… more
    Intra-Cellular Therapies, Inc (03/18/24)
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