PharmD, PhD
Founder & Research Director
"I am an epidemiologist with more than ten years of experience across academic research, real-world evidence generation in the CRO industry, and independent scientific consulting."
My Background
I hold a Doctor of Pharmacy from the Lebanese University and a PhD in Epidemiology from Sorbonne University in Paris, followed by post-doctoral research at CESP INSERM in France. I have authored more than 25 peer-reviewed publications in journals including Eurosurveillance, AIDS, the International Journal of Cancer, and the Journal of Allergy and Clinical Immunology: In Practice.
Most recently, I was Real World Evidence Research Manager at Oracle Life Sciences (formerly Cerner Enviza), where I led multi-country observational research programs from protocol design through to publication, working with interdisciplinary teams of researchers, analysts, and vendors.
Why I Founded EVIDASCIENCE
After more than ten years in academic research and in the CRO industry, I reached a point where I could take another role in another company, or start something of my own. I decided to start my own practice.
My experience covers two areas. The first is the science: designing studies, writing analysis plans, and publishing results. The second is the delivery: leading multi-country observational programs, managing vendors, timelines, and budgets. In most organizations, these two responsibilities belong to different people, and important details are lost between them. I founded EVIDASCIENCE to bring both together in a single practice.
I design the studies I deliver, and I stay involved from the protocol through to the final report. I work in close collaboration with my clients. I recommend the design best suited to the research question and explain its strengths and limitations, including what the study can and cannot demonstrate. My clients define the questions; my role is to build the study that answers them.
Areas of Expertise
Observational study design, protocol development, and end-to-end evidence generation.
Clinical study reports, protocols, manuscripts, and conference abstracts.
Analysis planning and execution, data quality control and validation.
Ethics submissions, study reporting, and evidence synthesis for regulatory bodies.
End-to-end delivery across multi-country programs — on time and on budget.
Selected Publications
Fiocchi A, Worm M, Wing-Kin Wong G, Mnif T, Reed S, Hleyhel M, et al.
Prevalence of IgE-Mediated Food Allergies in Children and Adults: Results from the Multinational ASSESS FA Study.
Journal of Allergy and Clinical Immunology: In Practice
Gupta R, Mnif T, Reed S, Hleyhel M, et al.
Methodology of the international cross-sectional prevalence and severity study of pediatric and adult IgE-mediated food allergies (ASSESS FA).
World Allergy Organization Journal
Hleyhel M, Popovici O, Leuștean M, et al.
Prevalence of chronic hepatitis C infection in the general population: results from a national survey, Romania, 2020 to 2023.
Eurosurveillance
Hleyhel M, Geller J, Sadou A, et al.
Prevalence of chronic hepatitis C infection in the general population: results from a national survey, Estonia, July to December 2022.
Eurosurveillance
El Khoury J, Saleh N, Lahoud N, Maison P, Hleyhel M.
Compliance to international guidelines and rational use of antibiotics in urinary tract infections in a country without national guidance: a cross-sectional study.
BMJ Open Quality
Hleyhel M, Belot A, Bouvier AM, et al.
Trends in survival after cancer diagnosis among HIV-infected individuals between 1992 and 2009 (FHDH-ANRS CO4).
International Journal of Cancer
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