• Associate Director, Regulatory CMC (Small…

    BeOne Medicines (San Mateo, CA)
    …professional to manage, evaluate, and complete regulatory projects consistent with company goals. This individual will be responsible for development of strategies, ... the assigned project. + Provide CMC regulatory review for clinical protocols and investigator brochures, etc. for the assigned project. + Provide comments on new… more
    BeOne Medicines (06/25/25)
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  • Director, Global Patient Safety Sciences…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …development RMPs, RMPs, etc.) and the review of clinical documents ( Investigator Brochures, protocols, clinical study reports, etc.) + Leads cross-functional Safety ... characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known...would impose undue hardship on the operation of the Company 's business. For roles in which the hired candidate… more
    Regeneron Pharmaceuticals (06/24/25)
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  • Archaeology Technician

    AECOM (Los Angeles, CA)
    ** Company Description** **Work with Us. Change the World.** At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, ... under the supervision of a Crew Chief, Field Director and/or Principal Investigator . Ideally, candidates should be southern California based as **field projects will… more
    AECOM (09/21/25)
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  • Clinical Coder III - Department of Neurosurgery

    University of Florida (Gainesville, FL)
    …options for both adults and pediatric patients. Our research labs and investigator -led initiatives and clinical trials are developing promising new treatments for ... by electronic submission through Epic checking website or by contacting insurance company via telephone. Determines if patient was an emergency admit, hospital to… more
    University of Florida (09/21/25)
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  • Senior Front-End Engineer

    Dynatrace (Allin, IL)
    …Your team is responsible for building the Security Investigator (https://www.dynatrace.com/hub/detail/security- investigator /) app for evidence-driven security ... **Compensation and Rewards** + We offer attractive compensation packages and company stocks with **numerous benefits and advantages.** Dynatrace is an Equal… more
    Dynatrace (09/20/25)
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  • Research Assistant, Institute of Environmental…

    Wayne State University (Detroit, MI)
    …as assigned * Upon request, perform other tasks requested by Principal Investigator to maintain a smooth operation of the laboratory. Perform collaborative projects ... functioning of the laboratory. * Maintain an amicable relationship with company /vendor representatives. * Receive shipments, restocks shelves and aliquots out… more
    Wayne State University (09/20/25)
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  • Clinical Research Supervisor (Oncology)

    Actalent (Orlando, FL)
    …the Research Institute, overseeing the conduct of industry-sponsored and investigator -initiated clinical trials. This role ensures compliance with trial protocols, ... US, Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard… more
    Actalent (09/19/25)
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  • Clinical Research Coordinator

    Actalent (Philadelphia, PA)
    …team to assist with study coordination and recruitment for investigator -initiated studies, multi-center research studies, and patient-oriented clinical and ... US, Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard… more
    Actalent (09/19/25)
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  • Senior Clinical Study Manager (Hybrid)

    Stryker (Fremont, CA)
    …post-approval, post-market surveillance, feasibility and/or marketing studies, and/or investigator -initiated studies. + Lead the development of project charters ... study management experience at the sponsor level (CRO or medical device company ); site-level experience will only be considered in conjunction with sponsor +… more
    Stryker (09/19/25)
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  • Clinical Research Associate - Sponsor Dedicated

    IQVIA (Parsippany, NJ)
    …available for filing in the Trial Master File (TMF) and verify that the Investigator 's Site File (ISF) is maintained in accordance with GCP and local regulatory ... (ICH) guidelines. * Good therapeutic and protocol knowledge as provided in company training. * Computer skills including proficiency in use of Microsoft Word,… more
    IQVIA (09/19/25)
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