Sr. Computational Statistician

Role Summary

Sr. Computational Statistician responsible for statistical analysis, collaboration with study personnel, and communication of results within regulatory and clinical trial contexts.

Responsibilities

• Collaborate with statistical colleagues and study personnel to provide input to statistical analysis plans, write reports and communicate results, assist/respond to regulatory queries.
• Assist in selecting statistical methods for data analysis, author sections of the analysis plan, and conduct the analysis once a reporting database is created.
• Collaborate with data management in planning and implementing data quality assurance plans.
• Maintain proficiency with SAS programming and statistical methodology and apply new methods as appropriate.
• Justify methods selected and implement previously outlined analysis plans.
• Conduct peer-review of work products from statistical colleagues.
• Use current technologies and tools for conducting clinical trial analysis.
• Assist in communicating study results via regulatory submissions and manuscripts, and communicate with key customers as needed.

Qualifications

• Master’s degree in Statistics, Biostatistics or MSPH with concentration in Statistics or Biostatistics.

Skills

• Proficiency in statistical programming languages/software such as SAS, R, Spotfire, etc.
• Interpersonal/teamwork skills for effective interactions
• Technical growth and application with solid understanding of statistics and statistical software
• Self-management skills with a focus on results for prompt and accurate completion of competing deliverables
• Creativity and innovation
• Demonstrated problem solving ability and attention to detail
• Data analysis, technology, and systems expertise