Cardiovascular Clinical Trials Coordinator

Cardiovascular-Associates-of-America; Columbus (GA); On-site; USD 50,000 - 65,000; Full time

Job summary

CVAUSA is seeking a detail-oriented Clinical Research Coordinator to lead trial coordination and site operations in Columbus, GA. The role collaborates with investigators, sponsors, and staff to ensure high-quality data and adherence to GCP/ICH guidelines.

The position emphasizes patient enrollment, regulatory documentation, and continuous process improvement in a fast-paced cardiovascular research environment.

Qualifications

• Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical assistant).
• Bachelor's degree in life sciences, healthcare, or clinical research preferred.
• Minimum of 1–2 years of clinical research experience with patient enrollment and study coordination.
• Strong organizational and time management skills.
• Knowledge of GCP, ICH guidelines, and regulatory requirements; CCRP preferred.

Responsibilities

• Coordinate all aspects of clinical trials including recruitment, screening, enrollment and follow-ups.
• Support day-to-day site operations while ensuring regulatory compliance.
• Collect, verify, and maintain clinical trial data with accuracy and timeliness.
• Serve as primary contact for sponsors, participants and study stakeholders.
• Assist with improving research workflows and study performance.

Skills

Detail-Oriented

Strong Communicator

Collaborative Team Player

Adaptable & Results-Oriented

Education

Bachelor's degree (life sciences/healthcare/clinical research)

Clinical research certification (CCRP)

Tools

Electronic Data Capture (EDC)

Regulatory documentation management

Job description

CVAUSA is seeking a detail-oriented Clinical Research Coordinator to lead trial coordination and site operations in Columbus, GA. The role collaborates with investigators, sponsors, and staff to ensure high-quality data and adherence to GCP/ICH guidelines.

The position emphasizes patient enrollment, regulatory documentation, and continuous process improvement in a fast-paced cardiovascular research environment.