Job Description
Cytel is seeking a Senior Biostatistician to support or lead Phase I–IV clinical studies within sponsor-driven environments. You will perform ad-hoc analyses, contribute to protocols, SAPs, and integrated summaries for submissions while collaborating with clinical and regulatory teams.
Ideal candidates have a Ph.D. or strong statistical background, 5+ years in pharma/biotech, and proven SAS and CDISC expertise to drive high-quality regulatory submissions and data interpretation.
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