Senior Biostatistician – Clinical Trials & Analytics

PowerToFly; North Chicago (IL); On-site; USD 120,000 - 180,000; Full time

Job summary

AbbVie is seeking a Senior Research Statistician to provide statistical support across clinical trials, safety, and GMA activities. You will work with multidisciplinary teams to advance medicines, design analysis plans, and ensure high-quality statistical outputs.

Strong SAS, R or Python skills, and experience in clinical trials are required. Role emphasizes collaboration, data interpretation, and publication of scientific findings, with an emphasis on rigorous methodology and clear

Qualifications

• MS (with 4+ years) or PhD in Statistics, Biostatistics, or a highly related field.
• Experience with SAS.
• Experience with R or Python.
• Experience with clinical trials.
• Able to perform statistical computations and simulations.

Responsibilities

• Contribute to design, analysis and reporting of clinical trials or other scientific research studies with details for programming implementation.
• Identify data collection instruments and report data issues or violations of study assumptions; provide programming specifications.
• Perform statistical analyses per the analysis plan and ensure timely, high-quality outputs in collaboration with programming teams.
• Develop strategy for data presentation and inference; ensure accurate interpretation in reports and publications.
• Collaborate with cross-functional teams; explain statistical concepts to non-statisticians and support product-team communications.

Skills

Statistical analysis

Clinical trial experience

Communication skills

Problem solving

Education

MS or PhD in Statistics/Biostatistics

Tools

SAS

R

Python

Job description

AbbVie is seeking a Senior Research Statistician to provide statistical support across clinical trials, safety, and GMA activities. You will work with multidisciplinary teams to advance medicines, design analysis plans, and ensure high-quality statistical outputs.

Strong SAS, R or Python skills, and experience in clinical trials are required. Role emphasizes collaboration, data interpretation, and publication of scientific findings, with an emphasis on rigorous methodology and clear