Provide research and administrative support for clinical research programs focused on patient-reported outcomes, quality of life, and patient experiences. Assist with qualitative and quantitative research activities, including literature and scoping reviews, qualitative data analysis, survey development, data management, and dissemination of research findings. Support the day-to-day operations of assigned studies and collaborate with research team members to advance study objectives, improve understanding of patient experiences, and contribute to research that informs clinical care and patient-centered outcomes. Help the team achieve program goals while safeguarding research subjects’ confidentiality and identity when working with personally identifiable information (PII) and protected health information (PHI). The role supports study coordination, accurate electronic data capture, research records and databases, study logistics, project meetings, and compliance with applicable institutional review board (IRB) and regulatory requirements. It requires a high school education or equivalent; no prior experience is required. CITI Training must be completed within 90 days of hire. Appropriate experience may substitute for education on an equivalent basis. Work involves light exertion transporting materials or equipment, but not for sustained periods. The work environment is environmentally controlled, with occasional exposure to dust, noise, temperature changes, or water and other liquids. The position requires the ability to detect and translate speech or other communication; occasional color discrimination and perception of relative distances may also be required.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED