High quality and well-prepared data can make the difference in a successful regulatory submission or disappointing delayed approval. Whereas a full-service CROs may see data as an afterthought, a niche data focused CRO such as Intellectt Inc brings expertise and quality to data capture, statistical analysis, and clinical trial reporting. From the design of a study through to final submission, trust that your data will be in safe hands with the clinical data experts.

  • Clinical Data Manager
  • SAS Programmer
  • Statistician/Biostatisticians
  • Clinical Trial Associate / Clinical Trial Managers
  • Clinical Research Associate