As the Senior Statistical Programmer, you will work with the Principal Technical Consultant and provide SAS programming expertise in data extraction from various databases, TLG programming, developing programming and validation specifications. You will provide hands-on expertise in programming SDTM and ADaM datasets to support various analyses and TLG Programming. You will be responsible for developing and maintaining programming and validation specifications for TLGs as per requirements provided by the
Biostatistician.
KEY TASKS & RESPONSIBILITIES
➢ Create and maintain SAS programs to produce outputs to support the analysis and reporting of clinical trials
➢ Develop analysis datasets for trial level reporting and integrated safety and efficacy activities
➢ Program and QC data listings, summaries and graphs as defined in SAP. If required,
validate the statistical models used for programming
➢ Develop re-usable utility macros in order to build a macro library to support programming tables,
listing and graphs for phase 1-4 clinical trial reporting
➢ Collaborate with the project team to ensure the deliverables are completed on time with high quality
➢ Create submission-ready standard data presentations and data sets using standard coding and following standard industry processes including SDLC
➢ Maintain all project documentation as required by SOP and Processes
➢ Ensure compliance with eClinical Solutions and industry quality standards, guidelines, and procedures