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The LPN Clinical Research Coordinator supports multiple clinical research studies and trials in inpatient and outpatient care units. In an expanded role, the coordinator helps assess patient suitability for research protocols and, under physician direction, sees patients in clinic and hospital settings to collect protocol-required data. The position includes direct patient care within study protocols and oversight of trial activities from feasibility assessment through follow-up and retention. This is a full-time position scheduled for 40 hours per week, typically 8:00 a.m. to 4:30 p.m. Travel to outreach clinics may be required as needed for patient care or upon request. Work is typically performed in an office environment. A minimum of three years of LPN experience is preferred; oncology and/or research experience is strongly preferred. Certified Clinical Research Professional (CCRP) certification will be required in the future, with details to be discussed during the interview.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed

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