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


  • Start: a.s.a.p
  • Rate: €45000 - €65000 per annum + benefits
  • Location: Paris, France
  • Type: Permanent
  • Industry: Pharmaceutical
  • Recruiter: Key People
  • Tel: +44 (0)1727 817 626
  • Fax: 01727 844 838
  • Email: to view click here
  • Posted: 2020-12-22 21:51:50 -

  • View all Jobs from Key People


Share Job