Biostatistics is CROS NT’s forte and the foundation of its heritage. CROS NT has delivered expert statistical analyses and programming across all phases of drug development and in a wide range of therapeutic areas for more than 15 years.
Whilst the needs of pharmaceutical, biotechnology and medical device companies may vary, the quality of data analysis is critical to determine the success of a trial. For this reason CROS NT has invested in a highly-skilled team of biostatisticians and SAS programmers, experienced in providing excellence and customizing plans for every project. In addition, each analysis is conducted using validated and standardized procedures in compliance with regulatory guidelines.The professionalism, collaboration and prompt response of our people are the foundations which enables CROS NT to provide excellent services and maintain the highest level of scientific integrity.
Lisa has been in her current role at CROS NT since 2003, also assuming the title of Project Manager. Her previous experience with CROS SAS was in the role of Statistician and Data Manager. 
