Celerion

Senior Clinical Statistical Programmer – UK

Celerion

full-time

Posted on:

Location Type: Remote

Location: United Kingdom

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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