Sr. Statistical Programmers, ICON Clinical Research LLC., North Wales, PA (option to work from home). Create, validate, execute, & generate statistical programs consisting of listings, safety, & efficacy outputs to include analysis datasets, tables, & figures. Create & finalize project or departmental level macros and programming specifications/mock-ups.
Responsible for leading programming deliverables for at least one study of moderate complexity and/or scope including effective resource planning, tracking, & work allocation to ensure project, timeline, & quality goals are consistently achieved.
Req’d: MS or equiv. in a quantitative or scientific discipline & 2 yrs relevant exp performing Stat Programmer role; 2 yrs exp w/CDISC ADaM datasets & standards; 2 yrs exp programming analysis datasets from specifications & creation of TLFs; 1 yr exp writing analysis dataset specifications for safety & efficacy; 1 yr exp w/Electronic Submission or ISS/ISE programming; 1 yr exp as study team programming lead or having been responsible for clinical study programming deliverables to include datasets & TLFs; 1 yr exp w/oncology related SAS programming; & 1 yr exp w/clinical data analysis programming for Phase II or III studies in the Pharmaceutical or Biotechnology industries or for CRO. Will also accept BS & 5 yrs of exp. Base & Clinical or Base & Advanced SAS cert req’d. Less than 5% international travel req’d.
Refer to code 018207.