Guillaume Charles
Site and MedTech Partnerships Lead at Milo Health
Driving innovation in European clinical trials through AI-powered solutions and strategic partnerships with MedTech companies and investigator sites.
Additional Role:
- Study Start Up and Feasibility Specialist – Eclevar MedTech
Clinical Operations Expertise:
- MedTech Clinical Trials – Site partnerships and feasibility assessment
- AI for Clinical Research – Next-gen EDC platform implementation
- Study Start-up – Site qualification and regulatory compliance
- European Trials – EU MDR, GCP, and regulatory frameworks
- Patient Recruitment – EDC optimization and site contracting
Mission at Milo Health:
Leading strategic partnerships with MedTech companies and clinical sites to accelerate trial implementation across Europe. Specializing in Milo’s AI-powered EDC platform featuring voice/image capture, risk prediction, and EHR integration to streamline trials and accelerate patient access to innovative treatments.
Professional Background:
- 5+ years in clinical operations across leading CROs (IQVIA, Fortrea)
- Clinical Project Management experience at Amgen
- Specialized in clinical trial design and EU regulations (MDR/GCP)
- Expert in site start-up, feasibility, and regulatory processes
Impact & Innovation:
Passionate about transforming clinical research through digital health innovation and AI integration. Actively engaged in healthcare innovation summits and regulatory convergence events, contributing to the evolution of MedTech clinical trials in Europe and beyond.