• Post Doctorate RA - Coastal…

    Pacific Northwest National Laboratory (Seattle, WA)
    …Northwest National Laboratory - Seattle (PNNL-Seattle) Office is seeking a highly motivated ** Post Doctorate RA ** to conduct coastal modeling research ... related to 1) marine energy resource modeling (wave, tide, ocean current and ocean thermal conversion) characterization using unstructured-grid models; 2) coastal biogeochemistry and plastic modeling. The selected candidate is expected to work with a… more
    Pacific Northwest National Laboratory (04/23/25)
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  • Post Doctorate

    New York University (Brooklyn, NY)
    …AI/robotics conferences like CVPR/ICRA/NeurIPS/etc., or top automation journals like IEEE RA -L, Automation in Construction, etc. * Evidence and/or interest in ... conducting multi-disciplinary research * Experience and/or interest in teaching and mentoring * Interest in proposal writing with the intent to establish a record of externally funded research The applicants' proposed research must span the lab's areas of… more
    New York University (04/23/25)
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  • Regulatory Affairs CMC Manager

    Amgen (New Albany, OH)
    The Regulatory Affairs CMC Site Team is responsible for input to the development and implementation of CMC regulatory strategies and activities for products ... team interfaces with the site (R&D and operations authors) coordinate preparation of regulatory filings, identification of issues and factors that may implicate a … more
    Amgen (02/23/25)
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  • Medical Director, Medical Affairs - Lung…

    AbbVie (Mettawa, IL)
    …compliance with regulatory and ethical standards. . Collaborate with Regulatory Affairs , Legal, Compliance, and Pharmacovigilance teams to ensure adherence ... onsite 3 days per week in Mettawa, IL. The Medical Director, Medical Affairs serves as a strategic medical and scientific expert within the organization, responsible… more
    AbbVie (04/11/25)
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  • Medical Director Pharmacovigilance, Rare Disease…

    Takeda Pharmaceuticals (Boston, MA)
    …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, ... and interpret safety data from various sources including non-clinical, clinical, post -marketing and scientific literature for assessment of benefit-risk profile and… more
    Takeda Pharmaceuticals (04/05/25)
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  • Medical Advisor (Oncology)

    AbbVie (San Juan, PR)
    …All clinical research / development activities for products under development, and for post approval commitments such as regulatory agency mandated trials, or ... for one or a cluster of countries into core medical affairs activities such as: healthcare professional/provider interactions (Payers, Patients, Prescribers, and… more
    AbbVie (05/01/25)
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