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procedures, and clinical visit workflows. Provide guided instruction on the use of EPIC/EMR SmartPhrases, flowsheets, intake templates, and other EMR tools to support accurate and efficient documentation
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manage data using REDCap, Epic, and Excel Track participation, consent status, and recruitment progress Ensure accurate and timely documentation of recruitment activities Administrative & Program Support
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, proper transport of samples has been employed, etc). Utilize EMR (Epic) and Outlook lab calendar to set up study lab collections and schedule upcoming couriers. Participate in weekly lab rotation, daily
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efforts, and follow-ups. Prepare and organize research study materials, including participant packets, consent forms, and regulatory documentation. Schedule study-related appointments and coordinate
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transport of samples has been employed, etc). Utilize EMR (Epic) and Outlook lab calendar to set up study lab collections and schedule upcoming couriers. Participate in weekly lab rotation, daily patient
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, and informed consent processes. Coordinate study enrollment and follow-up visits while maintaining compliance with IRB-approved protocols. Organizing follow-up visits, and scheduling research activities
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and department leadership in scheduling training or collaborative sessions with clinical and translational researchers. Provides training, constructs evaluative instruments, and conducts evaluations
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REDCap and electronic health records (e.g., Epic). Experience with regulations governing clinical research (CFR, GCP, HIPAA). Experience with statutes and guidelines relevant to regulatory affairs in
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counseling, or another social service field. Experience using the Microsoft Office Suite (Word, Excel PowerPoint, Outlook). Experience with electronic health records, Epic preferred. Preferred Qualifications
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). Experience with electronic health records, Epic preferred Experience in quality improvement Excellent organizational, written communication, and oral communication skills. Job Duties Outlined: Assess tobacco