• AUROBINDO (Durham, NC)
    …Dispensed. (We are#27 in 2010)Job OverviewCapable of performing characterization studies for inhalation products, particularly for metered dose inhalers (MDIs). ... methods. Prepares SOPs, protocols, and reports. Meets timelines. Performs studies according to the stage-appropriate quality system.Qualifications - Skills &… more
    HireLifeScience (08/26/25)
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  • BioAgilytix (Durham, NC)
    …(BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies -including project scope definition, proposal preparation, timelines, scheduling, ... Manager (BPM)/Principal Investigator (PI), overseeing all aspects of bioanalytical studies including project scope definition, proposal preparation, timelines, scheduling,… more
    HireLifeScience (08/12/25)
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  • Associate Dean for Research and Graduate…

    North Carolina Agriculture & Technical State Unive (Greensboro, NC)
    …seeks an experienced educator and researcher to serve as the Associate Dean for Research and Graduate Studies , starting preferably January 2023,or no later than ... initiatives to significantly expand the College's scholarly productivity and increase its research funding. The selected candidate is expected to work closely with… more
    North Carolina Agriculture & Technical State Unive (07/24/25)
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  • Project Lead Engineer Studies HVDC Control…

    Siemens Energy (Raleigh, NC)
    **Snapshot of a day** **As a Project Lead Engineer in Studies HVDC Control & Protection, you will work within a team of HVDC project management and engineering ... located in Raleigh.** **How You'll Make an Impact** + **Dynamic performance studies within tender and project execution of HVDC projects** + **Optimizing the… more
    Siemens Energy (08/15/25)
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  • Environmental Engineer 5 (Feasibility…

    CDM Smith (Greenville, NC)
    …* Working on a variety of assignments, which may include field studies , research investigations, construction oversight, data interpretation and evaluation, or ... construction oversight and quality control * Estimating remedial costs for feasibility studies * Authoring feasibility studies * Performing surface and… more
    CDM Smith (08/26/25)
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  • Clinical Research Associate 2

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …solutions and services in more than 110 countries and regions. **The Clinical Research Associate assists in the management of the clinical monitoring process to ... adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols. Ensures coordination of an accelerated study start-up… more
    Grifols Shared Services North America, Inc (08/08/25)
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  • Clinical Research Associate,…

    IQVIA (Durham, NC)
    IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience is a plus! ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...issues as appropriate. * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and… more
    IQVIA (07/04/25)
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  • Clinical Research Coordinator 2

    ICON Clinical Research (Rocky Mount, NC)
    Clinical Research Coordinator - Level 2 ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an ... **_This role is with Accellacare (https://www.accellacare.com/about) , part of ICON's clinical research network, where you'll play a key role in transforming the… more
    ICON Clinical Research (08/28/25)
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  • (Senior) Clinical Research Associate…

    IQVIA (Durham, NC)
    …Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines of communication with… more
    IQVIA (07/14/25)
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  • Clinical Research Coordinator

    Alaka'ina Foundation Family of Companies (Camp Lejeune, NC)
    …Camp Lejeune, NC. DESCRIPTION OF RESPONSIBILITIES: + Responsible for coordinating the research activities of assigned IRB-approved study protocols. Work is ... performance of duties, and to guide patients through a research protocol, maintaining and document contact with study...environment and recommend changes, as needed. + Ensures all studies performed are in accordance with the approved protocol… more
    Alaka'ina Foundation Family of Companies (06/07/25)
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