Principal Medical Writer

We are looking for a Principal Medical Writer who will turn complex clinical and safety data into clear, regulatory-ready documents. The ideal candidate will have a PhD or equivalent expertise and 5 years of clinical regulatory writing experience in the pharmaceutical industry.

Requirements

• Proven experience writing a wide range of clinical and regulatory documents
• Work effectively in matrix teams to deliver high-quality, fit-for-purpose documents
• Major contributor to planning and producing clinical dossiers for international regulatory submissions
• Managed projects of increasing scope and complexity with demonstrated effectiveness
• Strong technical, statistical, and IT skills with ability to interpret complex clinical data

Benefits

• Contract of employment
• Attractive reward package
• Life insurance and pension plan
• Private medical package with additional preventive healthcare services
• Sports cards
• Possibilities of development within the role and company’s structure
• Personalized learning approach
• Extensive support of work life balance
• Supportive community and integration events
• Modern office with creative rooms, fresh fruits everyday
• Free car and bike parking, locker rooms and showers