Clinical Data Interchange Standards Consortium (CDISC), Clinical Study Publications, Data Sets, Pinnacle, Procedure Development, Quality Control, Statistical Analysis System (SAS), Statistics, XML (EXtensible Markup Language)
LOCATION
King of Prussia, PA
POSTED
8 days ago
Sr. Clinical SAS Programmer – ACL Digital- KOP, PA Multiple Openings Proficient to write SAS codes to produce CDISC complaint 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; and Revise programs for corrections, enhancements, or system environment changes. Proficient to generate Pinnacle 21 reports, Define XML, Define PDFs, and Reviewers Guides; Assist in establishing standardized programming procedures and work instructions; Develop, enhance, evaluate, and validate standardized macros and utility programs and Ensure regulatory requirements are met through validation/compliance activities.This roles requires a masters in Biomedical Engineering, Biomedical Sciences, C.S., Technology or related discipline and 24 months exp. Email resumes to: hr.us@acldigital.com and ref job# 22566842