A company is looking for a Statistical Programmer II/III who is proficient in R for a permanent role.Key Responsibilities:Develop, validate, and maintain statistical programs using SAS for generating Tables, Listings, and Figures (TLFs)Perform data manipulation, analysis, and visualization using R/SAS and relevant packagesCollaborate with Biostatisticians and Data Management teams to support clinical study deliverablesRequired Skills & Qualifications:Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, or a related field3+ years of experience in statistical programming within the pharmaceutical/biotech industryHands-on experience with R programming in a clinical trial environmentGood understanding of CDISC standards (SDTM, ADaM)Strong knowledge of clinical trial data and regulatory requirements