Scientific and Medical Writer M/F

Responsabilities

• 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 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