Please send resumes to jeff.sprague@talentmine.net Senior SAS Programmer Responsible for Biostatistical SAS Programming in support of multiple clinical trials. Duties: Statistical analyses of clinical trial data Creation of ADaM datasets Design and develop computer programs for production of TLF and derived datasets Review of CRF, SAP, QC specs and Database Structures Develop and implement QA software Full and complete documentation Creation and use of Macros Design and implement analysis file structures. Review code written by other Programmers Provide technical support to SAS users Experience & Qualification: BS degree, preferably in scientific, or mathematics discipline Must have experience working with ADaM datasets & specifications 7+ years work experience as a SAS Programmer in a BioPharma and/or CRO setting Understanding of data structures, standard software and their implementation Knowledge of the drug development & Clinical Trial process (all phases) Knowledge of and experience with general regulatory requirements Ability to work independently and/or also be part of a team Good written and verbal communications skills Pluses: Experience at, or ability to represent team at cross-functional meetings Lead / mentoring experience Prior experience working from home Please send resumes to jeff.sprague@talentmine.net