icometrix is a fast-growing company focused on impacting the lives of people with neurological conditions through its unique AI solutions that assist radiologists and neurologists in the reading of brain MRI and CT scans. The headquarters are based in Leuven, Belgium, but icometrix already has a US team present.
Our customers include hospitals and pharmaceutical companies. The icobrain solutions for people with multiple sclerosis, Alzheimer’s disease & other forms of dementia, stroke, brain trauma, and epilepsy, are already impacting clinical care decisions in many hospitals worldwide. Recently, based on the submitted evidence by icometrix, a new CPT III reimbursement code was issued by the AMA in the US, which is driving adoption of icobrain as the standard of care significantly.
The icometrix team includes enthusiastic, team-oriented and multi-cultural colleagues with a range of technical and medical backgrounds. We enjoy an innovative and challenging working environment and are driven by our core values: impact, trust, collaboration, respect, and crazitivity.

• Coordinate clinical studies and trials towards generating optimal clinical and health economic evidence of the icometrix portfolio
• Boost our neuro-imaging services to support optimal engagement of radiologists, neurologists, or other physicians aligned with the evidence strategy of icometrix
• Take a pro-active lead in the evidence dissemination plan (including scientific writing)
• Manage milestones, deliverables, timelines, budget, and quality to allow optimal implementation of our imaging services and ePRO services.
• Monitor progress, report and present study status, timelines, budget and quality of your deliverables to the Project Team, Management and Customer.
• Lead study-specific decision-making, develop improvements for increasing study efficiencies and co-ordinate issue detection and resolution
• Coordination of external partners (sites, additional vendors, both sponsor related as icometrix related)
• GCP complaint delivery and assure optimal coordination and communication for optimal implementations
• Prepare and support potential audits and inspections
• Have a critical view on the study results and Reporting proactively to the Team Manager on critical study-related issues
• Monitor closely project related elements linked to data management, Risk assessment and execution, contribution for submission ethics committees
• Participate in the development and coaching of less experienced staf