Junior Statistical Programmer
Job Summary
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
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