Impactful Emergency Med Clinical Research Coordinator I

The University of Chicago

Chicago (IL)

On-site

USD 50,000 - 65,000

Full time

10 days ago

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Job summary

The University of Chicago is seeking a Clinical Research Coordinator 1 to manage day-to-day operations across community-based, clinical, and data-driven projects; handling IRB submissions and regulatory documentation; assisting with participant recruitment and enrollment; organizing qualitative interviews, focus groups, and stakeholder engagement activities; tracking study timelines and deliverables; and maintaining high-quality study data.

Qualifications

  • Minimum requirements include a college or university degree in a related field.
  • Experience with IRB/regulatory processes and documentation.
  • Experience with participant recruitment, enrollment, and data collection.
  • Experience with community-engaged research or community partnerships.

Responsibilities

  • Serve as a resource person or consultant within area of clinical expertise.
  • Maintain current protocols and SOPs; assist with study goals and timelines.
  • Coordinate participant enrollment planning; conduct QA activities and data analysis.
  • Liaise with medical staff, university departments, and partner organizations.
  • Prepare IRB submissions, educational materials, and reports for Investigators.
  • Ensure regulatory documentation and audits are ready; support regulatory inquiries.

Skills

Bilingual EN/ES
GCP & FDA rules
IRB familiarity
Data management
Communication skills

Education

Bachelor's degree in related field
Master's in public health / epidemiology

Job description

The University of Chicago is seeking a Clinical Research Coordinator 1 to manage day-to-day operations across community-based, clinical, and data-driven projects; handling IRB submissions and regulatory documentation; assisting with participant recruitment and enrollment; organizing qualitative interviews, focus groups, and stakeholder engagement activities; tracking study timelines and deliverables; and maintaining high-quality study data.

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