Cytel is seeking an experienced Principal Biostatistician to lead one or more Phase I–IV clinical studies within a sponsor-dedicated setting. You will shape integrated analytic strategies, supervise study design and SAP creation, and collaborate closely with cross-functional teams to drive regulatory submissions.
Ideal candidates bring 8–10 years of biostatistics experience in pharma/biotech, strong R and SAS skills, and a PhD or equivalent depth of expertise.
#J-18808-LjbffrSenior Principal Biostatistician & Clinical Lead employer: Cytel
Cytel is an exceptional employer that fosters a collaborative and innovative work culture, particularly for Biostatisticians dedicated to advancing Chemistry, Manufacturing, and Control (CMC) projects. With a strong emphasis on employee development, you will benefit from consistent training and support while working closely with a global pharmaceutical client at the forefront of patient treatment. This role offers the unique opportunity to contribute to meaningful projects in a dynamic environment where your expertise in Bayesian analysis can truly make an impact.
