Stephanie Fayolle
Clinical Data Transparency: Inclusive, strategic and inspirational leader always looking to improve processes and gain efficiencies.
- Role
- Associate Director External Data Sharing at Sanofi
- Location
- Bethlehem, PA, US
- LinkedIn followers
- 500 followers
About Stephanie Fayolle
I am an accomplished Clinical Trial Manager with over 20 years of experience in clinical data management, pharmacovigilance, data sharing, and business intelligence. I have a proven track record of leading high-profile projects, establishing robust governance structures, and ensuring regulatory compliance. I excel in collaborating with consortiums and external stakeholders to advance innovative treatments and improve patient outcomes. My expertise in project leadership, regulatory liaison, clinical data sharing, analytical reporting, quality control, and training has consistently driven operational efficiencies and enhanced data utilization across development projects. With leadership and pragmatic solutions, I have significantly contributed to the reduction of study backlogs, improvement of data sharing processes, and the successful implementation of business intelligence tools.My superpower is thriving in high-energy environments, shifting disorder to clarity and innovation.
Experience
Associate Director External Data Sharing
Dec 2016 — Present
As a Project Leader, I manage clinical trial data sharing, increase data utilization, lead process improvements, establish governance and quality control measures, and represent Sanofi in consortia.
Education
Université Claude Bernard Lyon 1
DIU, Investigateur aux essais cliniques des medicaments
2001 — 2002
Université Jean Monnet Saint-Etienne
Master's degree, Biologies des populations et des ecosystemes
2000 — 2001
Lehigh University
Master, Molecular Biology
2010 — 2012
Skills
- Clinical Trials
- Oncology
- Regulatory Affairs
- Good Clinical Practice (Gcp)
- Gcp
- Biopharmaceuticals
- Medicine
- Infectious Diseases
- Ich-Gcp
- Pharmacovigilance
- Gmp
- Meddra
- Clinical Research
- Vaccines
- Regulatory Submissions
- CRO
- Biotechnology
- Ctms
- Regulatory Requirements
- Clinical Development
- Pharmaceutical Industry
- Sop
- Fda
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