Job Description

Clinical R Programmer - Experienced Professional (5+ Years Experience) Overview: We are looking for an experienced Clinical R Programmer in combination with SAS with 5+ years of combined experience in R & SAS within the clinical research or pharmaceutical industry . The ideal candidate should have expertise in developing and validating ADaM datasets, tables, listings, and figures (TLFs) using R , along with a strong understanding of CDISC standards, clinical trial data processing, and regulatory compliance . Key Responsibilities: R Programming Tasks: Develop and validate ADaM datasets, tables, and listings using R . Work with R data structures (matrices, vectors, lists, data frames) for dataset creation and manipulation. Implement date formatting, character functions, and missing value handling in R. Utilize industry-standard R packages : DPLYR, TIDYVERSE, HAVEN, ADMIRAL, LUBRIDATE, STRINGR - Data manipulation and analysis. GGPLOT2 - Advanced data visualization. Perform dataset validation and comparisons (equivalent to PROC COMPARE in SAS). Debug and optimize R programs for performance and accuracy. Familiarity with R Markdown and R-Shiny for reporting (optional but preferred). Required Skills & Experience: 5+ years of combined experience in SAS and R programming in the clinical research or pharmaceutical domain . Proficiency in R programming for clinical data processing and visualization. Strong understanding of R packages (DPLYR, TIDYVERSE, HAVEN, etc.). Knowledge of CDISC standards (SDTM, ADaM) and regulatory submission requirements. Experience in debugging, dataset comparisons, and handling missing values in both R and SAS. This role is perfect for professionals looking to leverage both SAS and R programming skills in clinical research, ensuring compliance with industry standards and regulatory requirements . Send your Resume on [email protected] Job Category: Client Based - Sourcing Job Type: Full Time Job Location: Bangalore Chennai Remote