Epi Research Assistant, Research Dept CON
Rush University Medical Center
This job at a glance
- Who can apply
- New grads and up to 1 year · Diploma
- Must know
- OperationsRecruitingHIPAAGCPExcelMicrosoft Office
- Nice to have
- Patient careCustomer service
- Work
- On-site in Chicago
- Pay
- Not stated by the employer.
- Skill demand
- Operations27%Recruiting14%GCP8%HIPAA5%of 98 similar entry-level jobs posted in the US this week
- Listed
- Nov 8, 2026 · still open
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About the Role
The Epidemiology Research Assistant supports data collection, participant assessment, and research operations across epidemiological, behavioral, or population health research studies. This entry-level role focuses on participant support, data collection, study implementation, and logistical coordination guided by senior research staff and the principal investigator.
Key Responsibilities
- Participant Engagement
- Assist with recruitment, screening, and scheduling of participants based on eligibility guidelines under supervision.
- Support the informed consent and HIPAA documentation process using approved study materials and instructions.
- Data Collection & Entry
- Enter participant data accurately into study systems and assist with data checks or corrections as directed.
- Administer basic questionnaires and structured assessments following scripted instructions.
- Study Operations & Logistics
- Prepare and organize study materials (e.g., forms, kits, equipment) for participant visits.
- Monitor supply levels and notify senior staff when restocking is needed.
- Operate basic study equipment (e.g., tablets, sensors, blood pressure cuffs) after training.
- Documentation & Recordkeeping
- Maintain visit logs and review study forms for accuracy and completeness.
- Flag missing or inconsistent documentation and notify assigned team members for follow-up.
- Team Collaboration
- Attend team meetings and provide updates on assigned tasks or field activities.
- Complete required institutional and study-specific trainings before supporting independent duties.
- Other Duties As Assigned
- Support additional study-related or administrative responsibilities as requested by study leadership.
Requirements & Tech Stack
- Education: High school diploma or GED equivalent.
- 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.
- Other Duties as Assigned: Supports additional research-related activities as directed.
Qualifications (Preferred)
- Education: Associate degree OR 50+ college credit hours, OR equivalent gained through work or training.
- Experience: Experience supporting clinical, behavioral, community-based research studies or a customer service setting.