Statistical Programmer I / II

• You'll support statistical programming activities across clinical trials, ensuring high-quality and timely deliverables.
• This includes developing and validating SDTM and ADaM datasets, performing QC checks, and ensuring CDISC compliance.
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• A Master's or Ph.D. degree in Statistics, Biostatistics, Computer Science, or a related field.
• Approximately 3-5 years of experience in clinical trial statistical programming.
• Excellent knowledge of SAS is essential, with R considered advantageous.
• Good working knowledge of clinical data standards such as CDISC, SDTM, and ADaM.
• Understanding of TLFs, clinical data structures, and regulatory submission requirements.

• The opportunity to be involved in a growing organisation.
• Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
• Fully remote role within the UK.
• Competitive remuneration package.

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