Senior Clinical SAS Programmer Analyst
Senior Clinical SAS Programmer Analyst, Ms., degree, in Biotech., or CS., with 2 years., of experience; Work, on ICH, GCP guidelines, CDISC principles & Phase I-IV Clinical studies. Generate SAS reports according to 21 CFR-Part11. Create datasets in CDISC SDTM V 3.1.2 format. Analyze data sets (ADAM) to reflect specific, ADAM implement, guide & SAP. Use SAS/Macros in analysis of std., clinical data, generate & develop, Reports, Graphs, Listings, & Tables as per SAP, CRT’s, Reporting & Analysis datasets. Use OPEN CDISC validator to validate SDTM & ADAM datasets. Create datasets like TR/RS/TU & write specific, for database in CDISC format (STDM model 3.1) & NDA’s (ISS/ISE). Produce safety & efficacy reports- ISS & ISE for submission to Regulatory Affairs. Work, on ANOVA, Regression & correlation analysis. Must be willing to travel and/or relocate to work in unanticipated locations throughout the US.
We are an Equal Employment Opportunity (EEO) employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status or disability (in compliance with the Americans with Disabilities Act) with respect to employment opportunities.