Senior Statistical Programmer

Job Summary

Leading statistical programming activities, the full-time Senior Statistical Programmer will ensure the quality and efficiency of clinical trial data analyses, contribute to process improvements, and mentor junior staff, with the flexibility to work onsite in Dunkirk, NY, or remotely.

Key responsibilities

• Oversee the creation, validation, and maintenance of analysis datasets and statistical outputs
• Prepare electronic submissions of clinical trial data to regulatory authorities
• Provide guidance and training to junior staff on complex statistical programming techniques

Required qualifications

• Bachelor's Degree in Statistics/Biostatistics, Computer Science, Mathematics, or related field with 7+ years of relevant experience, or a Master's Degree with 5+ years of experience
• 5+ years of experience as a statistical programmer in the pharmaceutical industry
• Proficient in SAS and knowledgeable about CDISC STDM/ADaM guidelines
• Experience leading statistical programming projects concurrently
• Understanding of clinical research, Good Clinical Practices, and regulatory requirements