Helene Moutaffian

Helene Moutaffian is an experienced professional in regulatory medical writing, currently serving as the Director of Regulatory Medical Writing at Pierre Fabre Group since February 2017. Responsibilities include writing Clinical Trial Applications (CTDs), efficacy and safety summaries, and clinical overviews, particularly in the oncology field. With a solid background in medical writing spanning over ten years, Helene founded a medical writing company following a tenure as a Medical Writer. Previous roles include Director of Strategy at Vivactism2research and Scientific Director at Euraxi-capitole. Academic qualifications comprise a Ph.D. in Immunology and an MBA in International Marketing from Aix-Marseille University, along with two Diplomas from Bordeaux ISPED focused on regression methods and epidemiological practices.