Senior Medical Writer - Europe

I’m looking for 2 Senior Medical Writers based anywhere in Europe to work under the supervision of the Head of Medical Affairs Unit at a small-midsized CRO.

This senior medical writer will take ownership of a given assignment, proactively collaborating with biometrics staff, pharmacovigilance and the clinical operations units. Similarly to the medical writer they will be responsible for drafting, editing and reviewing preclinical/clinical documents such as preclinical and clinical study reports, study protocols, patient information and informed consent forms as well as other medical and regulatory documents (including Investigators’ Brochure, IMPD, Briefing Document for Scientific Advice and follow-up scientific advice, CTD).

Requirements:

• Fluent in English
• Master’s degree in biomedical/scientific disciplines
• At least 4 years of experience as medical writer
• Good knowledge of the drug development process, ICH-GCP guidelines and the methodology of clinical
• Knowledge of medical concepts and terminology

If you are interested in discussing this role in further detail please don’t hesitate to reach out to me:

roxanna.keshavarz@rbwconsulting.com / +441273 952187