Valérie Salentey

Valérie Salentey is the current Director of Regulatory Affairs & Quality Assurance at Sensorion. Valérie has held this position for 2 years and 4 months. Prior to this, they were the Head of Regulatory Affairs at NEOVACS SA for 1 year and 5 months. Before that, they were a Senior Regulatory Affairs Manager at PPD for 9 months.

Valérie began their career as a Trainee Clinical Trial Regulatory Affairs at Merck for 6 months. Valérie then became a Trainee administrator cell/gene therapy, biovigilance at Afssaps for 6 months. After that, they worked at Genethon for 4 years and 5 months as a Clinical Trial Regulatory Affairs Manager, Regulatory Affairs Specialist.

Most recently, they were the Regulatory Affairs and Quality Assurance Manager at CYTHERIS for 5 years and 7 months. In this role, they were responsible for global management of clinical trials Regulatory Affairs in EU, Switzerland and North America. Valérie was also a member of executive committee involved in product development and regulatory strategy, risk analyses and due diligence processes.

Valérie Salentey attended the Université Pierre et Marie Curie (Paris VI) for a CESAM in Statistic and clinical research diploma from 2006-2007. Valérie also attended the Université Claude Bernard (Lyon I) for a Hospital Residency in Pharmacy from 2003-2007. Valérie has a post graduated diploma from the Université Pierre et Marie Curie (Paris VI) in Molecular & Cellular Biology from 2002-2003. Lastly, they attended the Université Paris Cité for Pharmacy from 1997-2002.