Cardiology Clinical Research Coordinator II

Rush University Medical Center; Chicago (IL); On-site; USD 37,000 - 52,000; Full time

Job summary

Rush University Medical Center is seeking a Clinical Research Coordinator II to independently coordinate multiple clinical studies. You will recruit and retain participants, manage study data, and handle regulatory submissions with increasing autonomy.

The role supports protocol compliance and ongoing communication with sponsors and teams. Ideal candidates have 2+ years of trial coordination, strong regulatory knowledge, and the ability to travel locally for visits and training.

Qualifications

• Bachelor’s degree required; 2+ years coordinating clinical trials.
• Independent site management experience preferred.
• Knowledge of GCP and regulatory guidelines.

Responsibilities

• Coordinate all aspects of the study including recruitment, consent, screening and scheduling.
• Provide study updates to participants and team throughout the conduct of the study.
• Submit study-related documents to the IRB with increasing autonomy over time.
• Ensure documentation is compliant with local, state and federal guidelines.
• Monitor data accuracy and assist with study reports and audits.

Skills

GCP Knowledge

Regulatory Compliance

Study Coordination

Data Management

Regulatory Submissions

Communication Skills

Team Leadership

Travel Flexibility

Education

Bachelor’s degree

Job description

Rush University Medical Center is seeking a Clinical Research Coordinator II to independently coordinate multiple clinical studies. You will recruit and retain participants, manage study data, and handle regulatory submissions with increasing autonomy.

The role supports protocol compliance and ongoing communication with sponsors and teams. Ideal candidates have 2+ years of trial coordination, strong regulatory knowledge, and the ability to travel locally for visits and training.