- 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
Responsabilities
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