Job Description

Medix is hiring for Senior Level Clinical Research Coordinators in Downtown Chicago (60611)!

Job Description

The Clinical Research Coordinator independently manages clinical research projects, ensuring compliance with ethical standards and regulatory requirements. Responsibilities may include direct patient interaction and/or data management, depending on study needs.

Key Responsibilities

• Coordinate all phases of clinical studies (start-up through close-out), ensuring protocol and regulatory compliance.
• Manage site visits, sponsor communication, and regulatory documentation, including FDA submissions and study registration.
• Oversee participant engagement, including recruitment, consent, eligibility verification, and ongoing support.
• Maintain study documentation, supplies, and timelines; support budget and grant preparation.
• Collect, enter, and analyze study data while ensuring data accuracy and integrity.
• Train and mentor research staff; support onboarding and ensure adherence to SOPs.
• Contribute to research dissemination through publications, presentations, and educational events.

Qualifications

• Bachelor’s degree and minimum two years of research experience required.
• Experience with complex studies preferred.
• Strong organizational, communication, and analytical skills.
• Knowledge of FDA, HSR, and GCP guidelines.
• Leadership and mentoring experience; commitment to diversity and inclusion.

Additional Details:

• Location: Chicago, IL (60611)
• Schedule: Monday-Friday; Normal Business Hours; Onsite 5 Days a Week
• Pay: $62,000-$78,000 (Dependent on background and years of experience)
• Duration: ~6 month (1,040 Hours) contracted probationary period into direct hire / permanent position

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