Principal Statistical Programmer (Clinical Trials)

The Principal Stat Programmer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. Proficiency in SAS programming and familiarity with CDISC standards are required. The role involves developing and validating complex data sets and outputs, collaborating with cross-functional teams, and mentoring junior programmers.

Requirements

• Bachelor's Degree in Statistics, Computer Science or related field
• 2 + years working with efficacy analysis (ADaM datasets & TLF's) and/or 4 + years on ADaM statistical programming on clinical trials
• Experience in Immunology or Neuroscience therapeutic area highly valued
• Proficiency in SAS programming language
• Proficiency in R programming language
• English Advanced
• Ability to lead/manage others
• Demonstrated ability to maintain confidential information, sensitive project data and internal communications
• Exercises sound judgment and decision-making in selecting statistical methods and programming techniques
• Effectively manages time and resources to deliver high-quality programming outputs within tight deadlines
• Demonstrates robust technical aptitude with a deep understanding of SAS programming and CDISC standards
• Analyses and interprets financial data accurately to make informed decisions in statistical programming
• Applies effective problem-solving skills to overcome programming challenges and optimize workflows
• Exhibits strong written and verbal communication skills