• 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
  • Male or female with Post-graduate science degree in a biomedical field
  • Previous medical or scientific writing experience
  • Ability to analyse and summarise 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
Additionnal informations
  • Permanent position, available immediately
  • Based in Paris
  • Salary & package to define according skills and experience