Assoc Director, Statistical Programming

Role: Associate Director of Statistical Programming in clinical drug development, leading programming activities for complex global trials across multiple phases. Responsibilities include developing programming strategies, coordinating internal and external programming teams, ensuring quality and audit readiness, and driving standardization through innovative tools like R, R Shiny, and AI-enabled applications. The role involves cross-functional collaboration with Biostatistics and Data Management, resource management, and representing the programming function in project and submission teams.

Requirements: University degree in life sciences, data science, or related field; proven leadership and organizational skills; strong understanding of clinical trial methodology, GCP, and medical terminology; experience in drug development and statistical programming; ability to manage multiple trials and operate effectively in a global, fast-paced environment.

Preferred: Management experience, familiarity with modern programming tools and data visualization platforms.

High-Value: Focus on clinical trials (Phases I-IV), global project scope, emphasis on standardization, innovation in statistical programming, and cross-functional leadership. Located in East Hanover, USA, with no relocation support provided.