Senior Research Statistician, Early Oncology (Hybrid)
AbbVie
August 18, 2026
Remote friendly (Irvine, CA)
United States
$96,500 - $183,500 USD yearly
Clinical Research and Development
Major Job Responsibilities:
- Contribute to design, analysis, and reporting of clinical trials or other scientific research studies; assist with protocols and statistical analysis plans for programming implementation.
- Assist in identifying appropriate data collection instruments; identify/report data issues or study assumption violations; provide programming specifications for derived variables and analysis datasets; collaborate with Data Science for database lock.
- Perform statistical analyses per the analysis plan; collaborate with Statistical Programming to deliver high-quality outputs on agreed timelines.
- Develop strategy for data presentation and inference; ensure appropriate interpretation of statistical deliverables; collaborate in publication of scientific research; ensure accuracy/internal consistency of statistical components (tables, listings, figures).
- Work with cross-functional teams; explain statistical concepts to non-statisticians; respond to questions and pursue analyses suggested by data under supervision.
Qualifications:
- Minimum: MS (4+ years) or PhD in Statistics/Biostatistics or highly related field; ability to perform statistical computations and simulations; experience with pharma clinical trials; strong oral/written communication.
- Preferred: Experience in oncology.
- Required Skills: Build relationships with peers and cross-functional partners; motivated to drive innovation; identify data/analytical issues and help provide solutions (own skills or seek help).
Benefits (as stated): Paid time off; medical/dental/vision insurance; 401(k) for eligible employees; eligible for short-term incentive programs.
- Contribute to design, analysis, and reporting of clinical trials or other scientific research studies; assist with protocols and statistical analysis plans for programming implementation.
- Assist in identifying appropriate data collection instruments; identify/report data issues or study assumption violations; provide programming specifications for derived variables and analysis datasets; collaborate with Data Science for database lock.
- Perform statistical analyses per the analysis plan; collaborate with Statistical Programming to deliver high-quality outputs on agreed timelines.
- Develop strategy for data presentation and inference; ensure appropriate interpretation of statistical deliverables; collaborate in publication of scientific research; ensure accuracy/internal consistency of statistical components (tables, listings, figures).
- Work with cross-functional teams; explain statistical concepts to non-statisticians; respond to questions and pursue analyses suggested by data under supervision.
Qualifications:
- Minimum: MS (4+ years) or PhD in Statistics/Biostatistics or highly related field; ability to perform statistical computations and simulations; experience with pharma clinical trials; strong oral/written communication.
- Preferred: Experience in oncology.
- Required Skills: Build relationships with peers and cross-functional partners; motivated to drive innovation; identify data/analytical issues and help provide solutions (own skills or seek help).
Benefits (as stated): Paid time off; medical/dental/vision insurance; 401(k) for eligible employees; eligible for short-term incentive programs.