Statistical Programmer

• You'll lead statistical programming projects, ensuring high-quality, on-time deliverables.
• This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance.
• You'll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions.
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• A Master's or Ph.D. degree in Statistics, Biostatistics or Computer Sciences.
• At least 6 years' experience in clinical trial Statistical Programming.
• Excellent knowledge of SAS essential with R advantageous.
• Good working knowledge of data structures e.g. CDISC, SDTM, ADaM,
• Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines., About Our Client Experience, qualification, and soft skills, have you got everything required to succeed in this opportunity Find out below. Our client is a well-established and highly regarded specialist engineering business operating within the renewable energy and...

What in it for you:

• The opportunity to be involved in a growing organisation.
• Focus on career development and progression.
• Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
• Fully remote in the UK
• Generous remuneration package.

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