
Senior Clinical Statistical Programmer – UK
Celerion
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
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Job Level
Tech Stack
About the role
- Independently develop, maintain, and process SAS programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures.
- Perform peer QC, double programming and validation functions for statistical outputs from studies.
- Lead statistical programming activities on studies and deliverables.
- Assist Management and Biostatisticians with complex projects.
- Design and implement SAS programs for standardized use.
- Train and mentor junior programmers.
- Ensure compliance with study protocol and departmental procedures.
Requirements
- Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field.
- Minimum 3 years of hands-on statistical programming experience in a CRO or pharmaceutical clinical trials environment.
- Proficient in Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/ODS.
- Experience applying CDISC requirements to generate ADaM datasets and supporting documentation (define.xml, Reviewer’s Guides), demonstrating proficiency in these areas.
- Familiarity with Pinnacle 21 validation.
- Experience in early-phase clinical trials.
- Experience with Phase I Safety, PK/PD analysis programming.
- Excellent interpersonal skills.
- Strong problem-solving and decision-making abilities.
- Demonstrates a high level of attention to detail.
- Demonstrated ability to work collaboratively as part of a team.
- Familiarity with R, Python, and other programming languages is preferred.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
SASSAS MacrosSAS/STATSAS/GraphSAS/ODSADaMCDISCdefine.xmlReviewer’s GuidesPK/PD analysis
Soft Skills
interpersonal skillsproblem-solvingdecision-makingattention to detailcollaborative teamwork