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# Senior Clinical Statistical Programmer (Portfolio Development / Biometrics /Programming)

- **Company:** Csl
- **Location:** Reading, UK
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Biometrics, Computer Programming, SAS (Software), Information Technology, Programming Languages
- **Published:** September 27, 2026
- **Apply:** https://www.apply4u.co.uk/jobs/senior-clinical-statistical-programmer-portfolio-development-biometrics-programming/48375417

## About the Role

departmental tools and process improvements. Engage in ad hoc analytical work, including regulatory query responses, exploratory analyses, and publication support as needed.What We're Looking ForTo thrive in this role, you should have: Experience in programming within pharmaceutical, biotech, CRO, or clinical research settings. Strong proficiency in SAS (Base/Macro/Stat/Graph); familiarity with R or other programming languages is a plus. A working knowledge of current CDISC standards-CDASH, SDTM, ADaM, define.xml. A proven track record of producing and validating submission-ready TFLs and datasets, including ad hoc analytical requests. Experience supporting regulatory submissions (FDA required; PMDA, NMPA, or EMA experience is a bonus). Comfort in working with external vendors and CRO-managed data. A BSc in Computer Science, Mathematics, Statistics, or a related field; equivalent experience and certifications will also be considered.Why Join Us?At CSL, we believe
in fostering a collaborative and innovative environment where your contributions truly matter. You'll have the opportunity to grow your skills, mentor others, and make a significant impact on clinical trials that can change lives. If you're ready to take on this challenge, we'd love to hear from you!

## Description

behind it. Every regulatory decision-whether it's a safety signal caught or missed-depends on the quality of the datasets and outputs. In this role, you will be at the heart of this process, ensuring that everything is built right the first time. Your insights will help catch ambiguities early, preventing potential data issues down the line.Your ResponsibilitiesAs a Senior Clinical Statistical Programmer, you will: Lead end-to-end programming for your assigned studies, overseeing the full clinical development lifecycle from setup to regulatory submission. Design and validate SDTM and ADaM datasets, tables, figures, and listings in collaboration with study statisticians. Review and take ownership of CRO-produced deliverables, ensuring they meet submission-ready quality standards. Lead the specification and delivery of integrated analyses (e.g., ISS/ISE) and associated outputs when not handled by a CRO. Mentor less experienced programmers on internal processes and contribute to


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