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reports to identify and prescreen eligible patients to be presented with a consent forms for tissue bank studies. Build and maintain daily schedule to coordinate in-clinic or eConsent by data staff
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of clinical research data. May oversee the work of junior staff and train or mentor others in clinical research tasks. Research Operations. Knowledgeable in regulatory and institutional policies and processes
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consent plans and documents for participants in a variety of studies. May train or oversee others. Develops and submits documentation and information for IRB review. Communicates with the IRB staff and
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cord blood banking, data collection, and specialized laboratory procedures and techniques for the successful collection of umbilical cord blood units for public banking. An integral member of a team of
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meeting and speaking preparation, project development, travel, and other duties. Transmit instructions and/or information to and from staff members. Serve as liaison with internal and external agencies
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, update, and report study information according to project-specific scope of work and timelines. Critically assess trial processes, anticipate problems, and recommend improvements. Follow up, resolve, and
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to explain menu process and collect diet preferences. *Visit patients to obtain their menu selections and input selections into hand held computer. *Determine food preferences for patients on routine modified
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preferences. *Visit patients to obtain their menu selections and input selections into hand held computer. *Determine food preferences for patients on routine modified diets; order additional food items as
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Communicates with and educates physicians, mid-level providers, patient resource managers, case managers, Hospital Information Management (HIM) Compliance Specialists, and other health team members to facilitate
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. • Identify correct patient information in Maestro Care. Verify patient demographic data. • Edit Maestro Care as needed. • Accurately identify the appropriate account for patient visits. • Present and