Scientific and Medical Writer

• 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

• 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

experience in the preparation of marketing authorisation applications and regulatory responses

salary package to define according to skills and experience