IQVIA in Reading is seeking an experienced Biostatistician to lead the statistical strategy for clinical trials and regulatory submissions. The role requires a PhD or MS in Biostatistics or Statistics and at least 8 years of experience in clinical trial statistics. You will collaborate with cross-functional teams, represent Biostatistics in regulatory discussions, and effectively communicate results to stakeholders. Strong proficiency in SAS and R is essential, along with a proven ability in strategic study design and regulatory interactions.
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