Advisor - Computational Statistician

Responsibilities

• Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans, write reports and communicate results.
• Afford assistance/respond to regulatory queries.
• Select and respond to statistical methods for data analysis, author the corresponding sections of the analysis plan, and conduct 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.

Therapeutic Area And Systems Knowledge

• Understand relevant disease states in order to enhance the level of customer focus and collaboration.
• Ensure replication of tools and systems, where applicable and stay informed of technological advances.

Regulatory And Quality Compliance

• Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes, and training.

Qualifications

• Master’s degree in Statistics, Biostatistics, or MSPH with concentration in Statistics or Biostatistics, or relevant areas.
• 7+ years of statistical analysis/programming experience.