Senior Statistical Analyst - Programming - Oncology (Hybrid)

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience — and products and services in our Allergan Aesthetics portfolio.

About the role

The Senior Statistical Analyst is a key role in the research and development of new pharmaceutical products. The primary responsibilities include the analysis and reporting of clinical trial data and leading the statistical programming activities for clinical studies and projects with lower complexity. The Senior Statistical Analyst interfaces with Statistics, Data Sciences, Medical Writing, Regulatory Publishing, and Clinical Operations.

Responsibilities

• Leads the statistical programming activities for projects with lower complexity.
• Leads the statistical programming activities for studies.
• Develop SAS programs for the creation of ADaM data sets following CDISC standards.
• Develop SAS programs for the creation of Tables, Listings, and Figures.
• Validation of ADaM data sets, Tables, Listings, and Figures.
• Create specifications for the structure of ADaM data sets for individual studies and integrated data.
• Create documentation for regulatory filings including reviewers guides and data definition documents.
• Leads the development of standard SAS Macros and participates in the development of standard operating procedures.
• Provides oversight and mentoring of assigned Statistical Programmers and Statistical Analysts.

Qualifications

• Minimum Qualifications:
  • Bachelor's in Statistics, Computer Science, or a related field.
  • 8+ years of relevant experience in quantitative analysis (or 6+ with a Master's).
  • Experience with SAS Programming.
  • Experience leading programming for clinical trials.
• Preferred Qualifications:
  • Master's Degree in Statistics, Computer Science, or related field.
  • R Programming experience.
  • Oncology specific experience.

Skills

• In-depth understanding of SAS programming concepts and techniques related to drug development.
• Fundamental understanding of CDISC Standards.
• Fundamental understanding of the drug development process, including experience with regulatory filings.
• Ability to communicate clearly both orally and in writing.
• Ability to accurately estimate effort required for study-related programming activities.

Pay

The compensation range described is the range of possible base pay that AbbVie believes in good faith it will pay for this role at the time of posting, based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and may ultimately pay more or less than the posted range.

Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick).
• Medical, dental, and vision insurance.
• 401(k) to eligible employees.
• Eligibility to participate in short-term incentive programs.