Junior Statistical Programmer

To support clinical trial programming activities, the full-time Junior Statistical Programmer will assist in the development and validation of datasets, tables, figures, and listings while working collaboratively in a team environment. Key responsibilities Support the development and validation of clinical trial datasets and deliverables using SAS and/or R Assist with programming validation, quality checks, and the preparation of CDISC-compliant datasets for regulatory submissions Contribute to the development and maintenance of programming specifications and documentation while collaborating with senior team members Required qualifications Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, Engineering, Life Sciences, or a related discipline 0-2 years of experience in statistical programming, preferably in the pharmaceutical or clinical research industry Basic to intermediate knowledge of SAS and/or R, with familiarity in SAS Macro language preferred Understanding of clinical trial data and the drug development process Knowledge of CDISC standards, SDTM, and ADaM is preferred