WORK EXPERIENCE
VP Medical Software
CardioRenal 07/2022 – 06/2024
- Directed a multidisciplinary team of 9 members across two critical projects, managing a budget of $420k and ensuring compliance with ISO 13485, IEC 62304, and MDR standards through audits.
- Spearheaded the development of a comprehensive Remote Patient Monitoring System, enabling real-time monitoring gathering 1000+ measurements.
- Orchestrated the development of a Secure Cloud Information System ensuring storage and management of 400+ patients’ sensitive data.
- Overcame technical challenges ensuring scalability, interoperability, and data privacy for 4 different research centers.
Product Manager
Bioserenity 05/2021 – 06/2022
- Managed the development and launch of 3 integrated wearable medical device products of electrophysiological records remotely interpreted by HCPs.
- Implemented streamlined reporting processes, resulting in improved diagnosis accuracy and reduced turnaround time for 50+ prescribers in 10+ hospitals and clinics.
- Designed and implemented 5 new Care pathways workflows for 100+ patients monitoring and management, resulting in a 15% increase in patient engagement.
- Successfully oversaw cross-functional teams in the deployment of these products, meeting 100% of project milestones on time by managing comprehensive planning, budgeting, and prioritization efforts, ensuring alignment with company objectives and market demands.
Product Owner
CardioRenal 07/2018 – 05/2021
- Deployed a CE-marked, ISO 13485 certified cloud solution with Health Data Host, ensuring regulatory compliance and secure health data management.
- Designed and launched a cloud-based microservices architecture on AWS, supporting HL7 FHIR interoperability in POC mode, enhancing healthcare data integration.
- Developed an expert system for personalized medical recommendations, leveraging a clinical database of 55,000+ patients to improve patient care and clinical decisionmaking.
Medical advisor
CIC-P - CHRU Brabois 10/2016 – 03/2018
- Deployed a patient pre-screening assistance solution for clinical studies on a dedicated server, managing 200+ patients.
- Led the development and optimization of clinical trial procedures to gain regulatory approval and ensure efficient access to clinical statistics results.
- Provided expert guidance and insight on medical and clinical matters to support product development and regulatory compliance.
