5+ YOEB.S. preferred in math/stat/CS; 5+ years clinical trials experience in pharma/biopharma; strong SAS and CDISC skills; proficiency with Microsoft Office; experience writing, testing and validating analysis programs and familiarity with regulatory submission processes.
SAS, CDISC, EDC, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project
Gilead SciencesNASDAQ: GILD: Develops and sells medicines for life-threatening infectious diseases.
8+ YOEAdvanced statistical programming experience for clinical trials, regulatory submissions, SAS and CDISC expertise, leadership and project management in pharma/CRO.
SAS, SAS Macros, Microsoft Excel, CDISC, ADaM, SDTM, CDASH
2+ YOELead statistical execution for clinical programs, manage external statisticians/programmers, evaluate CDISC packages, proficiency in SAS and R, MS/PhD preferred, and minimum 2 years clinical trial experience.