Clinical Research Coordinator II — Independent Study Lead

Rush University Medical Center; Chicago (IL); On-site; USD 57,000 - 81,000; Full time

Job summary

Rush University Medical Center is seeking a Clinical Research Coordinator II to independently coordinate assigned aspects of clinical studies across disciplines. The role emphasizes recruitment, data management, regulatory documentation, and liaison with sponsors and departments to ensure study compliance.

Requirements include a Bachelor’s degree (or 3 years’ equivalent experience) and 2+ years coordinating trials, with awareness of GCP and NIH/FDA guidelines.

Qualifications

• Bachelor’s degree required.
• 2+ years of experience coordinating clinical trials.
• Independent site management experience.

Responsibilities

• Coordinates all aspects of the study including recruitment, consent, screening, scheduling, tracking, and provides study updates to participants.
• May collect and enter data into CRF/EDC systems and respond to queries in a timely manner.
• Prepare regulatory submissions with increasing autonomy to support regulatory management responsibilities.
• Ensures documentation is accurate and compliant with applicable regulations.

Skills

Regulatory knowledge

Regulatory compliance

Project management

Problem solving

Detail orientation

Vendor interaction

Communication skills

Teamwork

Flexibility

Travel readiness

Education

Bachelor's degree

Job description

Rush University Medical Center is seeking a Clinical Research Coordinator II to independently coordinate assigned aspects of clinical studies across disciplines. The role emphasizes recruitment, data management, regulatory documentation, and liaison with sponsors and departments to ensure study compliance.

Requirements include a Bachelor’s degree (or 3 years’ equivalent experience) and 2+ years coordinating trials, with awareness of GCP and NIH/FDA guidelines.