• Community Health Worker (Community Programs)…

    Johns Hopkins University (Baltimore, MD)
    …community site visits. This position will communicate regularly with the study team to discuss recruitment, enrollment, and K-HEARS intervention delivery activities ... logs. This position will be supervised by the bilingual study team community leads (community health worker coordinator and...including Word, Excel, and Outlook. + Familiarity with clinical studies or trials and IRB procedures a plus. Classified… more
    Johns Hopkins University (12/20/25)
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  • Sr. Research Project Coordinator (Health Policy…

    Johns Hopkins University (Baltimore, MD)
    …and helps translate findings from mental health, addiction, and health policy studies into actionable insights for policymakers and partners. **Specific Duties & ... or more senior research staff to ensure operational feasibility of proposed protocol/ study design. + Develop standard operating procedures and data collection forms… more
    Johns Hopkins University (12/19/25)
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  • Sr. Clinical Research Coordinator (Psychiatry…

    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 ... procedures, and applicable regulations. + Participate in developing the study budget. + Develop and oversee the implementation of...recruitment strategy for participants for one or more assigned studies . + Set up a data collection system and… more
    Johns Hopkins University (12/19/25)
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  • Clinical Project, Feasibility Analytics Manager

    IQVIA (Durham, NC)
    …cross-functional collaboration to ensure high-quality feasibility outputs that inform study planning and accelerate trial start-up. **Key Responsibilities** + Ensure ... with Global Program Leads (GPLs), Global Trial Leads (GTLs), and study teams to execute feasibility-related objectives. + Perform feasibility activities including:… more
    IQVIA (12/18/25)
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  • Clinical Research Institute RN

    CommonSpirit Health (Santa Maria, CA)
    …Research Institute. The incumbent has responsibility for the oversight of studies that explore complex medical diseases, which involve specialty and subspecialty ... injections, and other procedures appropriate within the RN scope of + Dispense study medication to research participants under the direction of the PI, and/or… more
    CommonSpirit Health (12/18/25)
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  • Clinical Research Coordinator II, Thoracic…

    Cedars-Sinai (Beverly Hills, CA)
    …area.** The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
    Cedars-Sinai (12/17/25)
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  • Assistant Clinical Research Coordinator

    Stanford University (Stanford, CA)
    …+ Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews ... to gather data, as needed. + Administer standard study questionnaires and tests, score test measurements and questionnaires,...accuracy. + Extract data from source documents for research studies as directed. Collect data and complete case report… more
    Stanford University (12/11/25)
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  • Heart Institute Clinical Research Associate I…

    Cedars-Sinai (Los Angeles, CA)
    …Research Program Administrator, or Research Nurse to coordinate and/or implement the study . This role evaluates and abstracts research data and ensures compliance ... the IRB. Provides limited patient contact as needed for study and assist with study budget and...Category** : Academic / Research **Job Specialty** : Research Studies / Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift**… more
    Cedars-Sinai (11/28/25)
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  • Clinical Research Coordinator II - Guerin…

    Cedars-Sinai (Los Angeles, CA)
    …role?** The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
    Cedars-Sinai (11/21/25)
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  • Clinical Research Associate Manager (Remote)

    Teleflex (Minneapolis, MN)
    …Research Associates (CRAs). This individual has knowledge and experience managing study activities from site selection, start-up, to close-out with adherence to ... * Manage a team of in-house and regional CRAs, providing guidance on study conduct, clinical operational and monitoring strategy, as well as professional growth. *… more
    Teleflex (11/20/25)
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