The Clinical Research Coordinator supports Alzheimer’s disease (AD) research studies through community outreach, participant recruitment, enrollment, and follow-up. Working closely with the Principal Investigator, Program Manager, research staff, and collaborating sites, the coordinator helps recruit participants for Alzheimer’s disease genetics research. The role includes conducting participant visits in community and residential settings; obtaining informed consent; collecting blood samples; administering cognitive assessments; and gathering family and medical histories. The coordinator also prepares and ships research specimens, participates in clinical classification meetings, and supports Institutional Review Board (IRB) submissions, regulatory compliance, and study documentation. The position requires strong judgment, organization, and communication skills, along with the ability to travel to participant locations and collaborating institutions locally, statewide, and nationally. Occasional non-traditional work hours may be required. The schedule is Monday through Friday, 8:30 a.m. to 5:30 p.m., with flexible hours; the position is full time at 40 hours per week.
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Job Type
Full-time
Career Level
Mid Level