Responsibilities Provide sound experimental design and data analysis expertise. Author the protocol statistical sections and generate statistical analysis plans and study randomization. Review and sign-off on relevant study documents and data management and programming deliverables. Prepare mockup tables, figures and listings. Determine analysis and data presentations specifications. Provide verification reviews on final tables, figures and listings. Perform analysis, interpret study results, and collaborate with study team to produce safety monitoring reports, interim and final reports, and publications. Represent the biostatistics function on project teams and in cross-functional meetings. Requirements: BA/BS in computer science, statistics, or math with 3-5 years of relevant experience. MA/MS in a related field or 2-3 years of experience. Experience in the support of clinical studies in a pharmaceutical or biotech industry setting. Understanding of statistical experimental design and analysis, clinical trial requirements. Understanding of regulatory guidelines that affect statistical deliverables. Excellent organizational and analytical skills. Excellent communication skills, both written and verbal. Flexible team player with ability to balance multiple projects and instructions often with competing deadlines. Creative self-starter with strong organizational, prioritization and interpersonal skills.