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 SAS Programmer - Raleigh, North Carolina, United States

Job information
Posted by: Veristat, LLC 
Hiring entity type: Other 
Work authorization: Existing work authorization required for United States
Position type: Direct Hire, Full-Time 
Compensation: ******
Benefits: See below
Relocation: Not specified 
Position functions: Computers - Other
Travel: Unspecified 
Accept candidates: from anywhere 
Languages: English - Fluent
Minimum education: See below 
Minimum years experience: See below 
Resumes accepted in: English
Cover letter: No cover letter requested
Job code: cJP08Q02h57hi411llZ0l44iOoh5WF / Latpro-3772157 
Date posted: Feb-07-2021
State, Zip: North Carolina, 27604


SAS PROGRAMMER for Veristat, LLC to work at our Morrisville, NC loc. Under Biostat, Sr.-level SAS Progr +/or Mgr, aid prog activities for CSRs, DSMBs, interim analyses, manuscripts, etc. Supp't stat prog of Stat Analysis Plan (SAP)-planned tables, data listings, + graphs for CSRs, integ summaries of safety + effic, ad-hoc analyses + elec sub deliverables (datasets, data doc, progs, prog table of contents + patient profiles). Supp't migration activities in creation of SDTM + prod of ADaM. Design/write prog specs based on consults. Convert specs to SAS code to gen datasets + tables, listings + figures outputs. Analyze SAS code to find causes of errors + revise progs. Write + maintain doc of changes to SAS code, progs + specs. Rev progs for corrections, enhancements or sys environ change. QC SAS progs for dataset, tables, listings + figs. Apply CDISC knowledge (SDTM + ADaM) stds to dataset prog. Assist in estab std prog process + work inst; devel, enhance, eval + valid std macros + util progs. Ensure reg reqs met through valid/compl activs. Create stat analysis outputs in supp't of final reports, abstracts, posters, manuscripts + other clin pubs. Support sys to prod elec reg submissions. Participate in proj dealing w/ assessment, design +/or impl of data standards (e.g., CDISC SDTM + CDASH). Perform Gap Analysis on studies req migration to CDISC standards to ensure all doc + datasets necessary to perform migration activities are present + without issue. Work w/ migration team + client to resolve any issues. Annotate CRFs per CDISC Impl Guideline for migration to SDTM. Create SDTM specs doc based on CDISC Impl Guideline. Follow standardized SDTM migration programming procedures to create SDTM-compliant SAS datasets + Define.XML docs. Create analysis datasets (e,g., ADaM) specs based on SAP or any study analysis algorithm. Good verbal + written com ability. May undergo background checks. Must have Bach in Technology, Stats, Pharmaceutics or another rel science or math field and 1 yr rel exp in SAS programming w/ clinical trial data. Also reqs skills in (1 yr exp): data analysis, regulatory reqs, and drug dev process. Apply at
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