Cytel seeks an experienced Senior Biostatistician to support or lead Phase I–IV clinical studies within a sponsor-embedded role. You will perform statistical analyses, help design studies, and collaborate with CROs and client teams to drive regulatory submissions.
The adecuado candidate holds a Master’s in statistics (PhD preferred) with 5+ years in pharma/biotech, SAS and R expertise, and a strong grasp of CDISC/ADaM standards.