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Clinical Research Assistant, Radiology & Imaging Science

University of Arizona

  • Tucson, AZ
  • 2 days ago
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    Skills

    • Analysis Skillsunmatched
    • Clinical Practices/Protocolsunmatched
    • Clinical Researchunmatched
    • Clinical Trialunmatched
    • Data Collectionunmatched
    • Data Qualityunmatched
    • Database Administrationunmatched
    • Documentationunmatched
    • Federal Laws and Regulationsunmatched
    • File Maintenanceunmatched
    • GCP (Good Clinical Practices)unmatched
    • IRB/IEC (Institutional Review Board/Independent Ethics Committee)unmatched
    • Informed Consentunmatched
    • Maintain Complianceunmatched
    • Operations Processesunmatched
    • Patient Admissionsunmatched
    • Patient Follow-upunmatched
    • Procedure Developmentunmatched
    • Radiologyunmatched
    • Regulationsunmatched
    • Reporting Skillsunmatched

    Description

    • Assist with prospective and retrospective research studies, identifying and screening eligible participants, supporting subject recruitment, scheduling study visits, and coordinating imaging-related research procedures.
    • Obtain and document informed consent by completing Informed Consent Forms (ICFs) in compliance with Good Clinical Practice (GCP) guidelines and institutional requirements.
    • Responsible for accurate data collection, abstraction, and entry into research databases, including REDCap, while maintaining data integrity and participant confidentiality.
    • Prepare and submit study documentation through the electronic Institutional Review Board (eIRB) system, assisting with regulatory maintenance, maintaining study files, and ensuring ongoing compliance with institutional, sponsor, and federal regulations.
    • Assist Pl in developing clinical trial protocols; provide clinical enrollment of patients in PI''s research trial; responsible for completing intake for patients and meeting IRB requirements including calling patients and meeting with them to discuss requirements for study and serve as patient resource for concerns and provide information; assist with patient follow-up calls and appointments.
    • Compile data/collection, and assist in preliminary analysis; maintain research database, assist senior lab members with writing summary reports and report findings to investigator; assist senior lab members in the development of written operating procedures for clinical trial; assist senior lab members with submitting required documentation to IRB.
    • Maintain and order supplies; assist with training of new team members, including students and junior lab members.
    • May assist on related research studies within the assigned lab, based on project needs and Pl direction.

    Numbers & Facts

    LocationTucson, AZ

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