• Clinical Research Coordinator - Department…

    Wayne State University (Detroit, MI)
    …screen, obtain informed consent, and enroll eligible participants according to protocol for clinical studies. Schedule and coordinate participant's study visits ... setting, including subject interviews, administering survey instruments, etc., per protocol requirement. Collect and record participants' study-related data into… more
    Wayne State University (06/01/25)
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  • Human Subjects Protection Scientist (Hsps) II Mid…

    Magellan Health Services (Fort Detrick, MD)
    …on a contract award. Serves as the administrative reviewer of protocol submissions in Post-Approval Oversight. Provides limited initial review support tasks ... all applicable human subjects protection regulatory requirements. + Timely reviews protocol submissions (and associated documents such as consent forms, IRB… more
    Magellan Health Services (05/21/25)
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  • Clinical Research Technician

    University of Michigan (Ann Arbor, MI)
    …limited to: **Technician Level** + Clinic Coordination + Understands clinical research protocol structure, associated lab manuals, etc. and how to interpret study ... all supported clinical trials and biorepositories.. + Ships research samples per protocol including coordinating with study sponsor's receiving sites via e-mail or… more
    University of Michigan (08/09/25)
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  • Research Nurse 1 (2 Years Fixed Term at 75% FTE)

    Stanford University (Stanford, CA)
    …assessing research participants, planning, implementing and evaluating care, administering protocol defined medications, treatments and vaccines in compliance with ... multi-site studies. + Conduct study participant evaluations according to the study protocol , assess adverse events, and apply triage and judgment to determine course… more
    Stanford University (08/07/25)
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  • Financial Clearance Specialist

    Logan Health (Bigfork, MT)
    …needed. + Determine and process pre-certification or referral requirements per protocol . + Communicate with providers regarding out-of-network barriers and document ... management policies. + Maximize collection of co-pays and other balances per department protocol . + Review and resolve accounts on hold to ensure timely billing. +… more
    Logan Health (08/01/25)
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  • Clinical Research Coordinator II, Hybrid

    Cedars-Sinai (Beverly Hills, CA)
    …providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating ... compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents… more
    Cedars-Sinai (08/01/25)
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  • Clinical Research Nurse PRN

    Houston Methodist (Houston, TX)
    …This position implements clinical research patient care via the research protocol . The CRN position works with the Performance Improvement department, sponsor, ... and coordinates with interprofessional team as written in the research protocol . Contributes to teamwork by consistently responding positively to requests for… more
    Houston Methodist (07/29/25)
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  • Research Support Specialist (N)

    University of Miami (Miami, FL)
    …on the status of research activities, and submits monthly activity logs for protocol .3. Organizes and coordinates community working group meetings for protocol ... for community partners and supervises and oversees research data collection at protocol venues in the community.5. Reviews study progress, identifies areas of… more
    University of Miami (07/27/25)
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  • Sr. Research Program Coordinator - #Staff

    Johns Hopkins University (Baltimore, MD)
    …or more senior research staff to ensure operational feasibility of proposed protocol /study design. + Develop standard operating procedures and data collection forms ... from protocol (s). + Develop consent form(s) for clinical trials based on protocol (s). + Prepare materials for submission to IRB. This includes completing… more
    Johns Hopkins University (07/26/25)
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  • Senior Analyst - Trial Analytics, Insights…

    Bristol Myers Squibb (Princeton, NJ)
    …and site performance analytics. + The Scientific track focuses on protocol logic, patient population sizing, eligibility criteria, and feasibility planning. ... taking ownership of trial forecasting models, feasibility analyses, and protocol analytics - always with the goal of helping...are not expected to be a therapeutic area or protocol expert on day one, but you will be… more
    Bristol Myers Squibb (07/25/25)
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