Rheumatology Clinical Trial Coordinator I

uchicago

Chicago (IL)

On-site

USD 50,000 - 65,000

Full time

9 days ago
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Job summary

The University of Chicago's BSD Rheumatology section seeks a Clinical Research Coordinator 1 to support PI-led trials within the Biological Sciences Division. You will coordinate daily trial activities, manage compliance, and assist with financial and personnel aspects.

Responsibilities include screening, enrollment, adverse event reporting, consent documentation, protocol submissions, patient education, site visits, and coordination with sponsors, IRB, and QA teams.

Qualifications

  • College or university degree in a related field is required.
  • Less than 2 years of related work experience is preferred.
  • Clinical research experience or relevant experience is preferred.

Responsibilities

  • Coordinate all aspects of trials including enrollment and adverse event reports.
  • Maintain documentation: informed consent, IRB approvals, CRFs and drug logs.
  • Plan patient schedules for procedures and visits.
  • Ensure SOPs are implemented per sponsor and regulatory specs.
  • Prepare protocol submissions and revisions.
  • Educate patients on procedures, visits, and potential side effects.
  • Attend site visits with sponsors and study meetings.
  • Recruit and interview potential study patients; may handle specimens.

Skills

Clinical Research Coordination
Documentation & Compliance
IRB & Regulatory Knowledge
Data Management
Study Coordination

Education

Bachelor's degree in related field

Tools

REDCap
OnCore
EPIC
Microsoft Word
Excel
Adobe Acrobat

Job description

The University of Chicago's BSD Rheumatology section seeks a Clinical Research Coordinator 1 to support PI-led trials within the Biological Sciences Division. You will coordinate daily trial activities, manage compliance, and assist with financial and personnel aspects.

Responsibilities include screening, enrollment, adverse event reporting, consent documentation, protocol submissions, patient education, site visits, and coordination with sponsors, IRB, and QA teams.

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