Senior 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.
• You’ll also create define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs.

• 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.

• 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.

Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.

Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients’ needs this growing organisation offers a flexible, dynamic, and entrepreneurial culture. With ongoing growth and exciting career opportunities, it’s the perfect place to advance your career.