Scientific and Medical Writer M/F

Responsibilities:Medical writing of all types of regulatory and clinical study documentation including Investigators’ Brochures, clinical study reports, and protocols.Preparation of regulatory responses to health authorities.Preparation of marketing authorisation applications (eCTD module 2).Simultaneously manage several projects and meet tight deadlines.Requirements:Male or female with a post-graduate science degree in a biomedical field.Previous medical or scientific writing experience.Ability to analyze and summarize data from a diverse range of indications.Advanced scientific writing skills.Experience in the preparation of marketing authorisation applications and regulatory responses would be advantageous.Fluency in written and spoken English.Based in Paris.Salary & package to be defined according to skills and experience. #J-18808-Ljbffr