*DUTIES: *Develop SAS computer programs supporting clinical trials.  Develop software applications or programs to use for statistical modeling and graphic analysis. Incorporate CDISC standards in creation of SDTM datasets and derivation of AdaM datasets, adhering to FDA ICH GCP guidelines.  Define analysis dataset specification, and generate tables, listings and graphs and per statistical analysis plan. Develop analysis dataset specifications and company standards policies.

REQUIREMENTS: Master's degree or equivalent in Pharmaceutical Information Systems, Pharmaceutical Chemistry, or related field with at least two (2) years of experience in job offered or related occupation such as Programmer Analyst.  Any suitable combination of education, training, or experience is acceptable.  Travel/relocation may be required.

*WORK LOCATION(S): *700 American Ave., Suite 102, King of Prussia, PA 19406 and other unanticipated locations nationwide. Travel/relocation required to various unanticipated client work locations nationwide for long or short durations and unknown frequency.

JOB POSTING DATES: 05/02/2024-06/07/2024