Assist Biometrics Department with developing tools and techniques for improving process efficiencies.
Performing quality assurance procedures on work performed by others.
Review statistical analysis plans and protocols.
Contribute to the development and documentation of analysis/clinical data set specifications, safety and efficacy analysis programming, as well as any ad-hoc programming requests.
Develop and maintain Programming standard and custom data listings, summary tables, and graphs as specified in statistical analysis plan.
Implement and follow the latest versions of CDISC, FDA guidelines, Good Clinical Practice, and other industry standards.
Provide input into case report form design, database structure design, and edit check development.