SENIOR DATA ANALYST (STATISTICAL PROGRAMMING)

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can’t wait to meet you!

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.
  Celerion Values: Integrity Trust Teamwork Respect
  Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability

ABOUT THE ROLE

Celerion is seeking a Senior SAS Data Analyst to join our North American Data Management and Biometrics team to provide statistical programming support for early-phase clinical research. In this role, you will independently design, develop, maintain SAS programs to support the analysis and reporting of clinical trial data.

THE PRIMARY RESPONSIBILITIES OF THIS POSITION ARE:

• 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.