• Clinical Trial Nurse

    IQVIA (Washington, DC)
    **Are you a Registered Nurse interested in Clinical Trial work?** IQVIA is looking for qualified Registered Nurses interested in community and clinical ... trial work to visit clinical trial patients in their homes. You will be responsible...or Nurses who already work part time. **Role of nurse during visit:** + Collecting samples and required information… more
    IQVIA (08/29/24)
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  • Clinical Research Nurse I - Lombardi…

    Georgetown Univerisity (Washington, DC)
    …with Clinical Research Coordinators, providing patient education about clinical trial participation, treatment, potential side effects, and required ... and Hackensack Meridian Health in northern New Jersey. The Clinical Research Nurse I serves as ...with Data Coordinator(s) to assure the documentation for the clinical trial is complete and accurate, assisting… more
    Georgetown Univerisity (08/30/24)
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  • Clinical Research Nurse Coordinator…

    Georgetown Univerisity (Washington, DC)
    …with Clinical Research Coordinators. + Provide patient education about clinical trial participation, treatment, potential side effects, and required testing. ... inquiry and making a difference in the world. Requirements Clinical Research Nurse Coordinator I, Center for...with Data Manager(s) to assure the documentation for the clinical trial is complete and accurate; assist… more
    Georgetown Univerisity (07/05/24)
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  • Research Nurse

    Guidehouse (Bethesda, MD)
    …approaches based on scope of practice and/or training. + Assures compliance of clinical trial objectives and endpoints. + Collaborates with health care members ... necessary interventions to address issues related to the patient population on a clinical trial . + Interacts with physicians and web-based referral sources to… more
    Guidehouse (08/03/24)
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  • Research Program Coordinator

    Johns Hopkins University (Baltimore, MD)
    …with consenting study participants and documenting the consent process. + Coordinates initial clinical trial study documents for review and approval by central ... + Participates in all mandatory meetings to develop increasing knowledge of assigned clinical trial and Registry requirements. + Maintains a protocol database or… more
    Johns Hopkins University (07/17/24)
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  • Site Research Assistant

    IQVIA (Columbia, MD)
    …(EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS) + Preparing and maintaining study files, ... a clinical environment or medical setting, eg clinical research coordinator, nurse , medical assistant, other...potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary… more
    IQVIA (08/06/24)
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