Clinical Research Coordinator I — Data & Participants, Chicago

Rush University Medical Center

Chicago (IL)

On-site

USD 32,000 - 45,000

Full time

2 hours ago
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Job summary

Rush University Medical Center in Chicago seeks a Clinical Research Coordinator I (CRC I) to support clinical research across multiple disciplines. You will work under direction from the PI or supervisor, handling participant recruitment, data collection, and regulatory documentation to ensure compliance and data accuracy.

This role emphasizes patient safety and adherence to study protocols. The CRC I executes defined tasks with supervision, contributing to study progress while aligning with

Qualifications

  • Bachelor’s degree required.
  • 0–2 years of experience in a research study or other relevant experience.
  • Two (2) years’ total experience, where 1 year is supporting or coordinating research studies (in lieu of a degree).

Responsibilities

  • Recruits, consents, screens, schedules, tracks and provides study updates to study participants throughout the conduct of the study.
  • Collects and enters data into study CRFs and/or electronic data capture; responds to queries in a timely manner; assists in preparing simple data summaries, reports, or charts.
  • Maintains accurate and complete procedural documentation including study participant and site level documentation in compliance with guidelines and regulations.
  • Verifies data against source documentation for accuracy prior to entry to ensure timeliness and audit readiness.
  • May collect, process and ship potentially biohazardous specimens.
  • Administers structured tests and questionnaires per study protocols; may utilize related technology.
  • Provides ongoing study status updates and responds to questions from PI, Administrator, department stakeholders, Sponsor and Compliance.
  • Maintains study flow by prompt communication with participants and coordination with study team.
  • Participates in auditing and monitoring visits; communicates unanticipated problems.
  • Works with PI(s), sponsor, compliance, clinical staff and/or manager to improve routine processes related to research conduct.

Skills

Time management
Problem solving
Attention to detail
Participant relations
Communication skills
Team collaboration
Flexibility
Travel readiness
Other duties as assigned

Education

Bachelor’s degree

Job description

Rush University Medical Center in Chicago seeks a Clinical Research Coordinator I (CRC I) to support clinical research across multiple disciplines. You will work under direction from the PI or supervisor, handling participant recruitment, data collection, and regulatory documentation to ensure compliance and data accuracy.

This role emphasizes patient safety and adherence to study protocols. The CRC I executes defined tasks with supervision, contributing to study progress while aligning with

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