Medical writers at this company work on a highly diverse range of projects including preparation of all types of regulatory and clinical study documentation. We are seeking talented and ambitious individuals for the roles of medical writer. Ideal candidates will have a 'can-do' attitude combined with excellent attention to detail and an ability to work under pressure. Main responsibilities will be to participate in the preparation of registration dossiers, responses to health authorities and other clinical study documentation.

Responsibilities include:
*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

Profile:
*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 marketing authorisation applications and regulatory responses would be advantageous
*Fluency in written and spoken English