MEDICAL WRITER | BIOTECH | PARIS

• Responsibilities include:
  
• Medical writing of all types of regulatory and clinical study documentation including clinical study reports, regulatory responses, marketing authorisation applications, and publications for scientific journals and conferences
  
• Preparation of regulatory responses to health authorities
  
• Preparation of marketing authorisation applications (eCTD modules)
  
• Assistance to other regulatory task, including but not limited to, electronic gateway submissions to health authorities and disclosure of trial information on publicly accessible websites.
  

Profil

• Previous medical or scientific writing experience
  
• Ability to analyse and summarise data from a diverse range of indications
  
• Advanced scientific writing skills
  
• Post-graduate science degree in a biomedical field
  
• Experience in the preparation of would be advantageous
  
• Fluency in written and spoken English