Biostatistics Associate Director (HYBRID)

Role: Biostatistics Associate Director supporting global medicines development through advanced statistical analyses in clinical trials and observational studies. Responsibilities include leading biostatistics projects, authoring SAPs and key reports, collaborating with cross-functional teams, contributing to regulatory interactions, and providing technical guidance on complex issues. Requirements: Ph.D. in Statistics or Biostatistics with 7+ years (Ph.D.) or 10+ years (Master's); expertise in SAS, R, and advanced statistical methods; experience with NDA/MAA submissions and regulatory interactions, particularly in USA/Europe. High-Value: Focus on drug development, including clinical trial design and analysis, with emphasis on regulatory submissions and real-world data investigations. Work setup: Hybrid or onsite; flexible arrangements.