Senior Principal Statistician

- Knowledge of clinical trial design and analysis, including experience with complex statistical methods and models, including statistical principles and methodology - Experience in using SAS and R; knowledge of other statistical applications and programming languages a plus - Knowledge of applicable regulatory requirements and guidelines, e.g., ICH Guidelines and drug development regulatory requirements as they relate to statistics - Ability to work in a fast-paced, flexible, team-oriented environment - Excellent interpersonal and communication skills (written and verbal) - Strong attention to detail with a view to bring studies to a quality conclusion - Flexible, positive, creative thinker with good communication skills - Ability to work without close supervision with well-developed time management skills - MS or MPH in statistics, mathematics, or a related discipline with > 4 years of experience in pharmaceutical or biotechnology industry, or PhD in statistics, mathematics, or a related discipline with > 2 years of experience in the pharmaceutical or biotechnology industry - Knowledge of drug development regulations pertinent to statistical analysis - Knowledge of the oncology or hematology therapeutic area is preferred - Bayesian and adaptive design experience is preferred - Proficient SAS & R programming skills, solid understanding of CDISC models and standards - Excellent writing and communication skills, demonstrated leadership abilities, and excellent interpersonal skills