Celerion is seeking a Senior SAS Data Analyst to provide statistical programming support for early-phase clinical research, aiming to help get drugs to market faster.
Requirements
- 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.
- Familiarity with R, Python, and other programming languages preferred.
Responsibilities
- 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 statistical analysis plan and departmental procedures.
Other
- Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing related field.
- 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.
