Clinical Research

• Recruit, screen, enroll, and obtain informed consent from study participants
• Maintain the volunteer database and manage recruitment efforts
• Coordinate and oversee research sessions, including participant scheduling, space reservation, staff training, and documentation
• Ensure compliance with study protocols, regulations, GCP, Ethics Committee requirements, and internal GEHC processes
• Maintain regulatory binders, source documentation, trackers, and other study materials
• Assist the Principal Investigator with Ethics Committee applications and submissions
• Conduct training and guide study staff
• Facilitate monitoring visits and prepare for audits
• Serve as the main point of contact for research volunteers and study staff
• Maintain consent areas and scan bays, order supplies, and track spending
• Implement process improvements and electronic compliance processes
• Support Research Program Integrators
• Serve as a subject matter expert for coordinators at global sites
• Manage in-house ultrasound scanning sessions for GEHC Ultrasound Businesses in Horten and Oslo
• Be physically present in Horten and Oslo during ultrasound scanning sessions

Explore Clinical Research Coordinator at GE HealthCare. Review requirements and application details.