Ultrasound Research Coordinator — In-House Trials

HC1316 GE Precision Healthcare LLC; Horten; On-site; NOK 550,000 - 700,000; Full time

Job summary

GE HealthCare is seeking a Clinical Research Coordinator to manage in-house ultrasound scanning sessions for GEHC Ultrasound Businesses in Horten and Oslo. The role supports the clinical evaluation of new ultrasound imaging techniques and ensures smooth study operations.

You will recruit and consent participants, maintain databases, coordinate sessions, ensure GCP compliance, and support site staff and ethics submissions.

Qualifications

• Bachelor's degree in social, life science, or research related fields.
• Minimum 1 year of clinical research experience.
• Outstanding organizational skills.
• Proficient with Microsoft Office (Excel, Outlook, Word).
• Meticulous attention to detail and excellent communication skills.

Responsibilities

• Recruit, screen, enroll, and obtain informed consent from study participants.
• Maintain volunteer database and manage recruitment efforts.
• Coordinate and oversee research sessions, including scheduling participants and documenting.
• Ensure compliance with study protocol, GCP, Ethics Committee requirements, and GEHC processes.
• Maintain study documentation including regulatory binders and trackers.
• Assist with Ethics Committee applications and submissions (new studies, Continuing Review, Amendments, Deviations, AE reports).
• Provide training and guidance to study staff; prepare for audits and ongoing monitoring.
• Serve as SME for coordinators at global sites executing similar protocols.

Skills

Organizational skills

Microsoft Office proficiency

Communication skills

Attention to detail

Education

Bachelor's degree in social, life science, or research related fields

Tools

Microsoft Excel

Microsoft Outlook

Microsoft Word

Job description

GE HealthCare is seeking a Clinical Research Coordinator to manage in-house ultrasound scanning sessions for GEHC Ultrasound Businesses in Horten and Oslo. The role supports the clinical evaluation of new ultrasound imaging techniques and ensures smooth study operations.

You will recruit and consent participants, maintain databases, coordinate sessions, ensure GCP compliance, and support site staff and ethics submissions.