Senior Research Statistician, Early Oncology (Hybrid)
AbbVie
August 18, 2026
Remote friendly (Florham Park, NJ)
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/or statistical analysis plans including programming implementation details (work under supervision).
- Assist in selecting 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 (with supervision); collaborate with Statistical Programming to deliver high-quality outputs on agreed timelines.
- Evaluate software appropriateness for planned analyses; assess needs for novel statistical methodology development.
- Develop strategy for data presentation and inference (with supervision); ensure appropriate interpretation of statistical deliverables; collaborate in publication of scientific research; ensure accuracy and internal consistency of statistical content (tables/listings/figures).
- Work with cross-functional teams; clearly explain statistical concepts to non-statisticians; answer questions and pursue analyses suggested by data (with supervision).
Qualifications:
- Minimum: MS (4+ years) or PhD in Statistics/Biostatistics or related field; ability to perform statistical computations and simulations; pharma clinical trials experience; strong oral/written communication.
- Preferred: Experience in oncology.
- Required Skills: Build strong cross-functional relationships; motivated to drive innovation; identify data/analytical issues and help solve via own skills or collaboration.
Benefits (explicitly stated): Paid time off; medical/dental/vision insurance; 401(k); eligible for short-term incentive programs.
- Contribute to design, analysis, and reporting of clinical trials or other scientific research studies; assist with protocols and/or statistical analysis plans including programming implementation details (work under supervision).
- Assist in selecting 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 (with supervision); collaborate with Statistical Programming to deliver high-quality outputs on agreed timelines.
- Evaluate software appropriateness for planned analyses; assess needs for novel statistical methodology development.
- Develop strategy for data presentation and inference (with supervision); ensure appropriate interpretation of statistical deliverables; collaborate in publication of scientific research; ensure accuracy and internal consistency of statistical content (tables/listings/figures).
- Work with cross-functional teams; clearly explain statistical concepts to non-statisticians; answer questions and pursue analyses suggested by data (with supervision).
Qualifications:
- Minimum: MS (4+ years) or PhD in Statistics/Biostatistics or related field; ability to perform statistical computations and simulations; pharma clinical trials experience; strong oral/written communication.
- Preferred: Experience in oncology.
- Required Skills: Build strong cross-functional relationships; motivated to drive innovation; identify data/analytical issues and help solve via own skills or collaboration.
Benefits (explicitly stated): Paid time off; medical/dental/vision insurance; 401(k); eligible for short-term incentive programs.