Clinical Research Coordinator
Core
Manage in-house ultrasound scanning sessions for clinical research to evaluate new imaging techniques.
Role type
Clinical Research Coordinator (IC)
Builds
Clinical research studies for GE HealthCare Ultrasound Businesses
Domain
Medical Devices / Ultrasound Imaging / Clinical Research
Required skills
Participant recruitment and screening, Informed consent management, Study protocol compliance (GCP), Regulatory documentation management, Ethics Committee application support, Staff training and guidance, Audit preparation, Process improvement, Microsoft Office proficiency
Preferred skills
CCRC or CCRP certification, Prior Clinical Research Coordinator experience
Technologies
Microsoft Office (Excel, Outlook, Word), Electronic processes
Responsibilities
Recruit, screen, enroll, and obtain informed consent from study participants; Coordinate and oversee research sessions including scheduling and space reservation; Ensure compliance with study protocol, GCP, and Ethics Committee requirements; Maintain study documentation and regulatory binders; Assist Principal Investigator with Ethics Committee submissions; Conduct training for study staff; Facilitate monitoring visits and prepare for audits; Maintain facilities and order supplies; Implement process improvements.
Seniority
Mid-level, hands-on IC