Job Summary

• The Senior Medical Writer is expected to work on assignments largely independently or for complex documents, under guidance of a mentor, facilitating delivery of the written assignments through proactive coordination of stakeholders to build content.
• Authors a range of clinical documents, including regulatory documents following defined templates, including but not limited to protocols, clinical study reports, NDA/MAA CTD submission documents, investigator brochures, briefing documents, and responses to regulatory authority questions.
• You will join a team that values respectful collaboration, continuous learning and accountability.

Matching Summary

Salary

Base: PLN 166,500 to PLN 277,500 gross; Bonus/Equity: potentially eligible for a bonus; Benefits: statutory benefits, private healthcare, additional paid days off, life insurance, private pension plan, fully paid parental leave & care of family member leave

Skills & Requirements

Key Requirements

• Up to 5 years clinical regulatory writing experience
• understanding of basic drug development
• knowledge of scientific methodology and statistical principles
• working knowledge of ICH/GCP
• Excellent English language skills

Work Rights