Onsite Cardio Clinical Research Coordinator - Schaumburg

Cardiovascular Associates of America - CVAUSA; Schaumburg (IL); On-site; USD 55,000 - 85,000; Full time

Job summary

CVAUSA in Schaumburg, Illinois is seeking a Healthcare-focused Clinical Research Coordinator to support cardiovascular trials from start to finish. You will coordinate patient recruitment, screening, enrollment, and follow-up visits, while ensuring protocols are followed and data is accurately captured and stored.

You’ll work with investigators, sponsors, and site staff in a fast-paced environment, maintain regulatory binders, and contribute to site operations and process improvements in our

Qualifications

• 1–2 years of clinical research experience including patient enrollment and study coordination.
• Knowledge of GCP, ICH guidelines and regulatory requirements.
• Strong organizational and time management skills.
• Cardiovascular medicine experience (preferred).

Responsibilities

• Coordinate all aspects of clinical trials including recruitment, screening, enrollment and follow‑up visits.
• Ensure study protocols are followed accurately and consistently.
• Support day‑to‑day site operations while maintaining regulatory compliance and study documentation.
• Collect, verify and maintain trial data with accuracy and timeliness.
• Serve as a primary point of contact for sponsors, participants and stakeholders.

Skills

Detail‑Oriented & Organised

Strong Communicator

Collaborative Team Player

Adaptable & Results‑Oriented

Education

Bachelor’s degree in life sciences/healthcare/clinical research

CCRP certification (preferred)

Tools

Electronic Data Capture (EDC) systems

Regulatory documentation management

Job description

CVAUSA in Schaumburg, Illinois is seeking a Healthcare-focused Clinical Research Coordinator to support cardiovascular trials from start to finish. You will coordinate patient recruitment, screening, enrollment, and follow-up visits, while ensuring protocols are followed and data is accurately captured and stored.

You’ll work with investigators, sponsors, and site staff in a fast-paced environment, maintain regulatory binders, and contribute to site operations and process improvements in our