Sr. Computational Statistician

Responsibilities

• Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans, write reports and communicate results.
• Aid in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the analysis plan, and conducting the actual analysis once a reporting database is created.
• Collaborate with data management in the planning and implementation of data quality assurance plans.
• Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods.
• Effectively justify methods selected and implement previously outlined analysis plans.
• Conduct peer-review of work products from statistical colleagues.
• Effectively use current technologies and available tools for conducting the clinical trial analysis.
• Assist in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers.

Qualifications

• Master’s degree in Statistics, Biostatistics or MSPH with concentration in Statistics or Biostatistics.
• 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.
• Demonstrated problem solving ability and attention to detail.
• Data analysis, technology, and systems expertise.