Clinical data preparation
Structure source data, develop mapping specifications, and support SDTM dataset programming against the study’s defined standards.
Clinical SAS programming, data preparation, analysis datasets, and reporting support for life sciences teams. Connect study requirements with the programmers and delivery support needed to execute them.
Discuss your requirementsWork is aligned to the sponsor’s specifications, statistical analysis plan, and agreed quality processes.
Structure source data, develop mapping specifications, and support SDTM dataset programming against the study’s defined standards.
Develop ADaM datasets and derivation logic from approved specifications, with traceability to the underlying source and tabulation data.
Program statistical reporting outputs from approved analysis plans and output shells. Review layout, population definitions, and calculation logic with the study team.
Support independent programming checks, log reviews, reconciliation, and documented resolution of discrepancies.
Organize SAS programs, macros, and repeatable data processing steps to support consistent execution and maintainability.
Recruit Clinical SAS programmers, statistical programmers, and clinical data professionals for defined project and ongoing team needs.
Confirm study deliverables, standards, source formats, and the analysis plan.
Align mapping rules, derivations, reporting shells, and programming conventions.
Develop datasets and outputs with agreed quality-control and review steps.
Provide code, specifications, review records, and agreed output packages.
Discuss a defined implementation, additional specialist capacity, or support for an existing environment. We align responsibilities, deliverables, access, and review expectations before work begins.
Share your scope, technical environment, and timing with our team.