Base: pln 166,500 to pln 277,500 gross; bonus/equi...
On-site
Clinical regulatory writing experience
Interpret clinical data
Ich/gcp knowledge
GlaxoSmithKline is seeking a Senior Scientific Writer in Poland, responsible for authoring various clinical documents and ensuring high-quality standards in medical writing. The role requires strong clinical knowledge and collaboration with diverse teams, offering opportunities for professional growth in a culture focused on patient impact and accountability
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
Match Score: 85
GlaxoSmithKline is seeking a Senior Scientific Writer in Poland, responsible for authoring various clinical documents and ensuring high-quality standards in medical writing. The role requires strong clinical knowledge and collaboration with diverse teams, offering opportunities for professional growth in a culture focused on patient impact and accountability.
Salary
Base: PLN 166,500 to PLN 277,500 gross; Bonus/Equity: eligible for a bonus (if applicable) and/or awards for exceptional performance; Benefits: statutory benefits in accordance with Polish law, private healthcare, additional paid days off, life insurance, private pension plan and fully paid parental leave & care of family member leave
Skills & Requirements
Must-have
clinical regulatory writing experience
interpret clinical data
ICH/GCP knowledge
proactive stakeholder coordination
drafting regulatory documents
Nice-to-have
ambitious for patients
accountable for impact
doing the right thing
continuous learning
respectful collaboration
Key Requirements
Up to 5 years clinical regulatory writing experience
Good understanding of basic drug development
Knowledge of scientific methodology and statistical principles