Principal Biostatistician

October 21

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Clinical Outcomes Solutions

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Patient Reported Outcomes • Health Economics and Outcomes Research • Clinical and Observational Research Design and Execution • Outcomes Regulatory Support • Statistics and Psychometrics

51 - 200

Description

• An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across your region. • You are excited and enthusiastic, motivate your teams to do great work and collaborate easily with your clients. • Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. • Our Principal Biostatisticians provide statistical and development support and influence for the associated client's trials providing expertise into processes, clinical development plans, concept sheets and protocols. • You will formulate integrated analytical approach to mine data sources, employ statistical methods, machine learning & deep learning algorithms to discover actionable insights and automate process for reducing effort and time for repeated use.

Requirements

• Master’s degree in statistics or a related discipline. Ph.D. strongly desired. • 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry. • Ability to work independently, demonstrate initiative and flexibility through effective and innovative leadership. • Attention to detail and quality focused, excellent interpersonal and communication skills, innovative, and collaborative behaviours • SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers. • Knowledge of R programming (R Shiny/Python)