An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, will lead Phase I-IV clinical studies across your region. You will be dedicated to a global pharmaceutical client that is driving the next generation of patient treatment, empowering individuals to work with autonomy and ownership. Our Principal Biostatisticians provide statistical and developmental support, influencing clinical trials by offering expertise in processes, development plans, concept sheets, and protocols. They may also oversee work supported by other vendors. You will formulate integrated analytical approaches, employing statistical methods, machine learning, and deep learning algorithms to discover actionable insights and automate processes to reduce effort and time. Responsibilities include designing, running, and analyzing A/B and multivariate hypothesis tests to optimize customer and patient experience. You will work with senior data science team members to present analytical content effectively, develop automation for analysis and insights, and manage your own projects while collaborating with team members. Additionally, you will independently identify research articles and apply methodologies to business problems. At Cytel, we support employee success through training, development, and support. Qualifications include a Master’s degree in statistics or a related discipline, 9+ years supporting clinical trials in the pharmaceutical or biotechnology industry, attention to detail, excellent communication skills, and collaborative behaviors. Required technical skills include SAS programming for QCing critical outputs and working closely with programmers, as well as knowledge of R programming (R Shiny) and Python. This is a mid-senior level, full-time position in Research, Analysis, and Information Technology. #J-18808-Ljbffr