Senior Statistical Programmer

What you will be doing: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.

What you will need: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.

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 UKGenerous 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.