Provide statistical programming support for early-phase clinical research at Celerion, designing, developing, and maintaining SAS programs to support analysis and reporting of clinical trial data.
Independently develop, maintain, and process SAS programs, 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 standardized SAS programs; train and mentor junior programmers; ensure compliance with the statistical analysis plan and departmental procedures.
Requirements
Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field.
4+ years of SAS® programming experience in a CRO or Pharmaceutical industry.
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.
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 preferred.