Regulatory Medical Writer

An excellent opportunity has arisen for a Medical Writer to join a pharmaceutical company based in Paris, specialising in the discovery, development, and commercialisation of novel targeted therapies, including cancer, chronic inflammatory diseases and neurological degenerative disorders.



You will work on a highly diverse range of projects including preparation of all types of regulatory and 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 is essential


• Ability to analyse / 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

For further details, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@keypeole.co.uk