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Rush·Rush University Medical Center · Chicago, IL

Epi Research Assistant - Rush Institute for Healthy Aging Oak Lawn

Full timeDays
iPosting details
ScheduleDays · Full time
EducationHS diploma/GED · Associate degree preferred
SourceRush · posted Sep 10, 2026
✓Requirements
Education
✓High school diploma or GED equivalent
✓Associate degree OR 50+ college credit hours, OR equivalent gained through work or training
Qualifications
✓Regulatory Knowledge – Understands the purpose of Institutional Review Boards (IRB), HIPAA, and basic Good Clinical Practice (GCP) principles.
✓Regulatory Compliance – Follows established research procedures and maintains participant confidentiality under supervision.
✓Project & Time Management – Supports timely completion of assigned tasks and study visits.
✓Problem-Solving & Judgment – Recognizes field-related concerns and alerts appropriate team members.
✓Detail & Organization – Assists with organizing materials and maintaining accurate records.
✓Communication Skills – Communicates clearly and respectfully with participants and team members.
✓Computer Skills – Familiarity with Microsoft Office Suite (Word, Excel, PowerPoint) and/or Google Suite.
✓Teamwork – Cooperates with others and accepts direction from more experienced staff.
✓Flexibility – Willingness to shift tasks or adjust schedule based on study needs.
✓Travel Readiness – Ability to travel to off-site data collection sites using personal transportation, if required.
✓Experience supporting clinical, behavioral, community-based research studies or a customer service setting
+Rush University Medical Center
598beds
ChicagoIL
Pay for this position
Employer-posted
$17.63 – $24.91/hr
Apply to RushContact Recruiter about this role
✓You’ll need
Education
✓High school diploma or GED equivalent
✓Associate degree OR 50+ college credit hours, OR equivalent gained through work or training
Qualifications
✓Regulatory Knowledge – Understands the purpose of Institutional Review Boards (IRB), HIPAA, and basic Good Clinical Practice (GCP) principles.
✓Regulatory Compliance – Follows established research procedures and maintains participant confidentiality under supervision.
✓Project & Time Management – Supports timely completion of assigned tasks and study visits.
✓Problem-Solving & Judgment – Recognizes field-related concerns and alerts appropriate team members.
✓Detail & Organization – Assists with organizing materials and maintaining accurate records.
✓Communication Skills – Communicates clearly and respectfully with participants and team members.
✓Computer Skills – Familiarity with Microsoft Office Suite (Word, Excel, PowerPoint) and/or Google Suite.
✓Teamwork – Cooperates with others and accepts direction from more experienced staff.
✓Flexibility – Willingness to shift tasks or adjust schedule based on study needs.
✓Travel Readiness – Ability to travel to off-site data collection sites using personal transportation, if required.
✓Experience supporting clinical, behavioral, community-based research studies or a customer service setting
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About the role