معرفی
Hélène Roussel is a Clinical Study Coordinator affiliated with the University of Limoges and works within the Department of Pharmacology, Toxicology, and Pharmacovigilance at the School of Medicine and Pharmacy. She is based at the INSERM UMR 1248 research unit and the CRBioLim Biological Resource Center, where she manages clinical research coordination and logistical aspects of biological collections.
- PhD in Sciences (Biochemistry and Molecular and Cellular Biology) from INRA, Dijon (1999)
Her research focuses on clinical study management, regulatory compliance in pharmacovigilance, and multi-scale modeling of local pharmacokinetics. She specializes in developing clinical trial protocols, coordinating international studies, and ensuring adherence to ethical and legal standards in clinical research.
Roussel's work involves close collaboration with laboratories and regulatory bodies, including the preparation of budgets, documentation, and monitoring of biological sample collections at the CRBioLim center. She has expertise in pharmacokinetic modeling and personalized medicine, with a focus on clinical toxicology.
- Current role since 2006 at INSERM UMR 1248
- Previously worked at AstraZeneca, Danone-Vitapole R&D, and INRA
