Associate Biostatistician
Tasks
- Conduct statistical analyses for clinical trials
- Design and validate statistical methodologies
- Develop statistical programming and analysis plans
- Generate clinical trial reports
- Perform statistical validation and quality control
- Prepare statistical summaries for regulatory submissions
Perks/Benefits
- Employee Assistance programmes
- Health and Wellbeing Programmes
- Learning and development opportunities
- Life assurance and disability coverage
- Retirement and pension plans
Skills/Tech-stack
Clinical Trial Design | Clinical trial | Quality Control | R | SAS | Statistical Analysis | Statistical Reporting | Statistical validation | Trial design
Education
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Statistical Programmer II PLN 200K-259KADaM | Analysis Plan | Audit Readiness | Clinical Trial Data | Clinical dataWork from homeMid-level Full TimeWarsaw, Poland R1mo ago