Clinical Research Coordinator - Neurology Movement Disorders
Listed on 2026-01-03
-
Healthcare
Clinical Research -
Research/Development
Clinical Research
Job Description
Location:
Chicago, Illinois
Business Unit:
Rush Medical Center
Hospital:
Rush University Medical Center
Department:
Neurological Sciences-Res Adm
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (7:00:00 AM - 3:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://(Use the "Apply for this Job" box below).).
Pay Range: $23.12 - $32.66 per hour
Rush salaries are determined by many factors including, but not limited to, education, job‑related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
The Clinical Research Coordinator I supports neurology movement disorder research studies under the direction of the research manager and primary investigators, working collaboratively with a team of peer clinical research coordinators.
Job Summary:The Clinical Research Coordinator I (CRC I) supports the conduct of clinical research studies across a range of disciplines. Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s). Responsibilities include participant recruitment and interaction, study data collection and entry, maintenance of study and regulatory documentation, sponsor communication, and adherence to study protocols and policies. The CRC I executes defined study tasks with guidance, ensuring operational compliance, accurate data entry, and participant safety.
Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Job Qualifications:
- Education: Bachelor’s degree
- Experience: 0‑2 years of experience in a research study or other relevant experience
- OR
- Experience (in lieu of a degree):
Two (2) years’ total experience, where 1 year is supporting or coordinating research studies - Knowledge, Skills, & Abilities:
- Time Management – Ability to meet deadlines and manage assigned study tasks.
- Problem‑Solving – Ability to troubleshoot routine field issues and use discretion to elevate appropriately when unplanned events arise.
- Attention to Detail – Strong attention to accuracy in data collection and documentation.
- Participant Relations – Ability to build rapport, navigate sensitive topics, and maintain participant confidentiality.
- Communication Skills – Effective verbal and written communication skills with participants and internal study teams.
- Team Collaboration – Ability to collaborate within multi-disciplinary team settings and follow established workflows.
- Flexibility – Availability to work evenings, overnight shifts, or weekends if required by study protocols.
- Travel Readiness – Availability for local travel as necessary.
- Other duties as assigned.
Job Qualifications:
- Experience: Two (2) or more years prior experience in clinical research or related field.
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