Job TitleDUTIES:Proficient to write SAS codes to produce CDISC compliant datasets.Create statistical analysis outputs to be used in support of final reports, abstracts, posters, manuscripts, adhocs and other clinical publications.Write QC SAS programs for Dataset, Tables, Listings, and Figures following the departmental QC procedures and good programming practices.Write programs for ISS, ISE and pooled datasets.Revise programs for corrections, enhancements, or system environment changes.Proficient to generate Pinnacle 21 reports, Define XML, Define PDFs, and Reviewers Guides. Review Pinnacle 21 report for action needed to fix errors and warnings.Assist in establishing standardized programming procedures and work instructions.Develop, enhance, evaluate, and validate standardized macros and utility programs.Ensure that regulatory requirements are met through validation/compliance activities.Use and promote use of established standards, SOP and best practices.JOB REQUIREMENTS:Master's degree Statistics, Computer Science, Engineering or related discipline24 months experienceEmail resume to:
SR. CLINICAL SAS PROGRAMMER in king of prussia at Unknown Company
This position is listed as full time and onsite.