5+ years of relevant experience in SAS programming for Clinical trials
Strong knowledge of preparations for NDA filings, ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodologies.
Experience of extracting, manipulating, merging, summarizing, analyzing and presenting data using SAS procedures
Strong experience of base SAS programming, Proc SQL, macro programming, ODS and various SAS modules:
Strong experience in SAS programming in various phases of clinical trial.