Create, validate, execute, and document SAS programs that produce outputs (analysis datasets, tables, listings, and figures) from clinical trial data.
Produce special outputs to comply with regulatory requests, DSMBs, and similar situations.
Works effectively within SDTM and ADaM environment.
Effectively use SAS data step programming, various procedures, additional SAS methodologies such as macros, ODS, and SQL, and advanced programming methodologies such as SAS/STAT and SAS/Graph.
Provide status reports on projects and flag issues or risks to lead.
Read specifications, SAPs, and related documents, and translate into programming specifications.
Ensure that documentation and specifications are correct.
Fulfill project responsibilities at the level of lead for single complex studies or group of studies
Provide advanced technical expertise independently bring project solutions to Clinical Programming department, for complex studies.