• Clinical Research RN

    Dignity Health (Phoenix, AZ)
    …protocols from IRB preparation through query and data seal; ensuring protocol and regulatory compliance. Principal Duties and Responsibilities: + Participate in ... study development including protocol review, informed consent review and create study tools...+ Ensure the trial is conducted according to the protocol , ICH/GCP and FDA guidelines. + Administer study treatment… more
    Dignity Health (10/03/25)
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  • Research Nurse

    Catholic Health Services (West Islip, NY)
    …communicating with sponsors and submitting the requested information + Communicates the protocol schedule for each patient, including but not limited to the ... the relevant clinical team. Adheres to and complies with protocol specific requirements + Assists PI with the identification...and standards of practice + Attends and participates in protocol site initiation visits and any other applicable sponsor… more
    Catholic Health Services (10/03/25)
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  • Bus Manager - Temporary/Miscellaneous

    Gwinnett County Public Schools (Suwanee, GA)
    …federal, state, and local laws, GCPS policies and procedures, and GCPS Transportation protocol to protect the student passengers, the general public, and the school ... and procedures of the Gwinnett County Public School district and the protocol and regulations detailed in the GCPS Transportation Handbook.d. Operate bus free… more
    Gwinnett County Public Schools (10/02/25)
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  • Advanced Practice Professional (NP/PA), Clinical…

    Atlantic Health System (Morristown, NJ)
    …patient and caregiver education with regard to investigational products/devices and protocol requirements. + Serves as an advocate for patients. + Responsible ... at the appropriate committee meetings (if department required), Communicates all protocol requirements with the healthcare team. Obtains documentation of such… more
    Atlantic Health System (09/30/25)
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  • Research Support Specialist

    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 (09/27/25)
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  • Open Rank Clinical Research Coordinator (Entry…

    University of Colorado (Aurora, CO)
    …clinical staff, and research staff to ensure study procedures are performed per protocol and properly documented. + Ensure protocol specific compliance and ... perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies. + May be called upon… more
    University of Colorado (09/25/25)
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  • Clinical Research Coordinator 1

    University of Miami (Miami, FL)
    …of manuscripts. The CRC 1 will ensure that studies are conducted according to protocol design and will report deviations as they arise, and maintain study files such ... simple clinical research protocols. Maintains enrollment procedures according to the protocol . + Coordinates routine activities of clinical studies including data… more
    University of Miami (09/24/25)
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  • MRI Technologist - Per Diem

    EvergreenHealth Monroe (Monroe, WA)
    …volumes, dosage, and concentrate to perform examinations consistent with exam protocol and or Radiologist directions. Competent with venipuncture. Participates in ... positioning devices, and other accessory apparatus to perform imaging studies within the protocol . Must be able to lift, carry, and file patient folders weighing up… more
    EvergreenHealth Monroe (09/23/25)
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  • Clinical Research Coordinator C

    University of Pennsylvania (Philadelphia, PA)
    …obtaining informed consent in accordance with GCP standards and completing protocol -required source documentation and case report forms (CRFs). Outside of subject ... CRC-C will provide input from a study coordination perspective on protocol feasibility, grant planning, and development of regulatory materials, working… more
    University of Pennsylvania (09/20/25)
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  • Clinical Research Coordinator A

    University of Pennsylvania (Philadelphia, PA)
    …training (eg, electronic databases, specimen processing/shipping) and participate in protocol -specific training as needed. + Recruitment and informed consent. Assist ... institutional requirements. + Schedule and coordinate study visits and protocol -required assessments.Schedule participant visits within protocol -defined windows… more
    University of Pennsylvania (09/19/25)
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