About Mathieu
- Team & Project Leadership
- RWE/HEOR Strategy Development & Implementation
- Subject Matter Expert in biostatistics and pharmacoepidemiology
- RWE Study & Program Leadership
- People & Line Management
- Cross-Functional & Matrix Collaboration
- Evidence Generation Strategy
- Market Access & Medical Affairs Interfaces
- Real-World Evidence (RWE)
- Biostatistics, Data Science
- HEOR & Outcomes Research
- Pharmacoepidemiology & Epidemiology
- European Data Privacy, Regulatory Frameworks
- PRAC (EMA) for Post-Authorisation Safety Studies (PASS).
- HAS (French HTA) for non-interventional post-inscription studies (HDH/CESREES, CNIL MR004/006, CNAM).
- Europe: Chart reviews, HCPs and patients’ surveys, Pharmacies longitudinal prescription claims, France: Claims (SNDS, PMSI), diseases registries, chart reviews / Germany: Claims (SHI), EMR / UK: CPRD-HES; / Spain: SIDIAP.
- US: Claims (MarketScan, PharMetrics)
French
Native or bilingual
English
Fluent
Experience
- IndependantAdvisor - Real World Evidence & HEORPHARMACEUTICALS INDUSTRYJanuary 2025 - Today (1 year and 5 months)Barcelona, SpainI provide strategic RWE and HEOR services to pharmaceutical, biotech, and med tech companies, at both global and European affiliate levels.Key Roles
- Team & Project Leadership
- Strategy Development & Implementation
- Subject Matter Expert in RWE, HEOR, and Epidemiology
- Alira HealthDirector Real World EvidenceJanuary 2021 - December 2024 (3 years and 11 months)Barcelona, SpainKey Responsibilities:
- Lead and manage a team of RWE consultants (5–10 professionals)
- Advise clients as an RWE subject matter expert on study design, methodologies, and data source assessment
- Ensure operational excellence across multiple projects
- Plan, organize, and manage resources to ensure successful delivery of project objectives
- Business development for European RWE consulting services
- IQVIAEngagement ManagerMarch 2018 - December 2020 (2 years and 9 months)Paris, FranceKey Responsibilities:
- Lead the development of RWE study deliverables, including study protocols, statistical analysis plans, statistical analysis validation documents, statistical reports, and final study reports
- Manage European PASS projects based on secondary data sources (claims, EHRs, registries), designed and conducted in compliance with EMA (PRAC) requirements
- Plan, organize, and manage resources to ensure the successful delivery of project objectives
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Education
- M.Sc., Public Health, Methodology and statistics in biomedical research:Paris-Saclay University2002M.Sc., Public Health, Methodology and statistics in biomedical research:
- Bachelor of Science in Public HealthPaul Sabatier university2001B.Sc., Public health: