• UAS Test Range Manager

    Sigma Design (Pendleton, OR)
    …Primary Function: The Test Range Manager is responsible for the safe and coordinated operations of UAS at the Eastern Oregon Regional Airport (PDT) and within the ... sensitive data and reduce information security occurrences. + 1. Operations Management Plans, directs and coordinates daily range ...and taskings to UAS Range Engineer, UAS Range Ops Specialist , and UAS Office Specialist . Duties and… more
    Sigma Design (07/31/25)
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  • Principal Medical Writer

    Sanofi Group (Cambridge, MA)
    …in a timely manner for study start, conduct and completion, as well as regulatory submissions according to company standards and procedures with the ultimate aim ... cross-functional relationships with local and counterparts in other departments, especially Regulatory Operations . + Maintain awareness of current clinical… more
    Sanofi Group (07/31/25)
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  • Global Trade Compliance Manager

    Kuehne+Nagel (Union City, GA)
    …Contract Logistics Specialist at Kuehne+Nagel, you will manage end-to-end warehousing operations for our customers. By doing so with precision, you not only ... success of your team, but also to the day-to-day operations and success in the warehouse and distribution centres....trade and committed to maintaining the highest standards of regulatory integrity? Join our team as a **Global Trade… more
    Kuehne+Nagel (06/26/25)
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  • Future Opportunities- Join Our Talent Pipeline…

    AbbVie (North Chicago, IL)
    …of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + Oversees the conduct of clinical ... scientific and medical activities with internal stakeholders (ie, commercial, clinical operations , discovery, statistics, regulatory , etc ) as they relate… more
    AbbVie (07/04/25)
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  • Clinical Research Scientist, Medical Development

    Lilly (Indianapolis, IN)
    …documents such as protocols, informed consent documents, final study reports, and submissions (eg, annual reports) according to the agreed upon project timeline. + ... and conduct (for example, ethical review board, informed consent, regulatory approval/notification) consistent with Good Clinical Practices (GCPs) and local… more
    Lilly (08/04/25)
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  • Sr. Principal Scientist - TS/MS Device & Packaging

    Lilly (Indianapolis, IN)
    …including procedures, deviation investigations, technical reports, change controls, regulatory submissions , validation protocols and summary reports, ... mission to deliver life-saving medications to patients worldwide. As a Specialist in Technical Services/Manufacturing Sciences (TS/MS), you will provide technical… more
    Lilly (06/13/25)
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  • Scientific/Medical Director, Medical Affairs…

    AbbVie (San Francisco, CA)
    …of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + Has overall responsibility for ... scientific and medical activities with internal stakeholders (ie, commercial, clinical operations , discovery, statistics, regulatory , etc ) as they relate… more
    AbbVie (07/26/25)
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  • Research Administrator II (Post Award)

    Beth Israel Lahey Health (Boston, MA)
    …implementation of research business practices that establish effective and efficient administrative operations . This role is a wonderful opportunity to be part of a ... and translate financial data so it is understandable for the non- specialist . Investigate any anomalies and provides timely resolutions. Reallocate budgets and… more
    Beth Israel Lahey Health (06/25/25)
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  • Laboratory Supervisor, CMCF

    Dana-Farber Cancer Institute (Boston, MA)
    …Harvard Medical School-affiliated hospitals. + Perform the duties of a Lead Specialist approximately 95% of the time. + Staff Supervision: Overseeing and ... of cell processing protocols, ensuring efficiency, scalability, and adherence to regulatory standards. Is responsible to insure alignment between Sponsor and CMCF… more
    Dana-Farber Cancer Institute (07/08/25)
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  • Future Opportunities- Join Our Talent Pipeline…

    AbbVie (North Chicago, IL)
    …of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + Has overall responsibility for ... scientific and medical activities with internal stakeholders (ie, commercial, clinical operations , discovery, statistics, regulatory , etc ) as they relate… more
    AbbVie (07/04/25)
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