Onsite Miami Cardiovascular Clinical Research Coordinator

Cardiovascular Associates of America - CVAUSA; Miami (FL); On-site; USD 65,000 - 90,000; Full time

Job summary

CVAUSA in Miami is seeking a detail‑oriented Clinical Research Coordinator to support cardiovascular trials onsite. You will work with investigators, sponsors, and clinic staff to coordinate trials, manage data, and ensure regulatory compliance in a fast‑paced setting.

The role requires 1–2 years of clinical research experience, knowledge of GCP/ICH guidelines, and a healthcare background (RN, technologist, or similar). CCRP certification is a plus.

Qualifications

• Bachelor’s degree in life sciences, healthcare, or clinical research required or preferred.
• Minimum 1–2 years of clinical research experience including patient enrollment.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• CCRP certification preferred.

Responsibilities

• Coordinate all aspects of clinical trials including patient recruitment, screening and follow-up visits.
• Support day-to-day site operations while ensuring regulatory compliance and protocol adherence.
• Collect, verify and maintain trial data with accuracy and timely entry.
• Serve as primary liaison with sponsors, investigators, and site staff for updates and reporting.
• Maintain up-to-date study documentation and regulatory binders per GCP/ICH guidelines.
• Identify opportunities to improve research workflows and study performance.

Skills

Detail-Oriented

Strong Communicator

Collaborative Team Player

Adaptable

Education

Bachelor’s degree in Life Sciences or Healthcare

Clinical Research Certification (CCRP) preferred

Tools

Electronic Data Capture (EDC) systems

Regulatory documentation management

Job description

CVAUSA in Miami is seeking a detail‑oriented Clinical Research Coordinator to support cardiovascular trials onsite. You will work with investigators, sponsors, and clinic staff to coordinate trials, manage data, and ensure regulatory compliance in a fast‑paced setting.

The role requires 1–2 years of clinical research experience, knowledge of GCP/ICH guidelines, and a healthcare background (RN, technologist, or similar). CCRP certification is a plus.