Biostatistics Associate Director (HYBRID)

Role: Biostatistics Associate Director providing advanced statistical analyses to support drug development in a biopharma setting. Responsibilities: lead statistical work for multiple clinical trials or RWD investigations, author study SAPs, contribute to CSRs, develop analysis methods, and collaborate on regulatory interactions. Represent biostatistics in cross-functional teams, review programming specifications, and contribute to methodological publications. Requirements: Ph.D. in Statistics or Biostatistics with 7+ years of experience; expertise in SAS and R; extensive knowledge of statistical methods in drug development; prior staff management experience preferred. High-Value: involvement in NDA/MAA processes, direct engagement with regulators, global medicines development, and a hybrid/onsite work setup with flexible scheduling.