Clinical Research Coordinator

Role: Clinical Research Coordinator supporting innovative healthcare research initiatives, focusing on ultrasound device studies. Responsibilities: recruit, screen, and consent study participants; coordinate study activities including scheduling, documentation, and facility management; ensure compliance with protocols, GCP, IRB standards, and internal processes; manage regulatory submissions and documentation; train and guide research staff; serve as main contact for study volunteers and staff; facilitate audits and monitor visits; implement process improvements and electronic systems; support global site coordination as SME. Requirements: Bachelor's in science or related field; minimum 2 years clinical research experience; strong organizational and communication skills; proficiency in Microsoft Office; meticulous attention to detail. Preferred: CCRC or similar certification from ACRP/SOCRA; prior coordinator experience. High-Value: healthcare research, clinical trial compliance, IRB submissions, GCP, ultrasound-focused studies, onsite in Beachwood, OH, with no specified travel.