Statistical Programmer (Hybrid)

AbbVie; North Chicago (IL); Híbrido; USD 70 000 - 110 000; Tempo integral

Resumo da oferta

AbbVie in North Chicago, IL is seeking a Statistical Programmer supporting clinical research. You'll develop and validate SAS programs for ADaM datasets, tables, listings, and figures, contributing to regulatory documentation.

You'll consolidate diverse data sources, perform exploratory analyses and visualizations, and collaborate with Statistics, Data Strategy, Medical Writing, and Regulatory Publishing teams to ensure accurate, compliant analyses for drug development.

Qualificações

• MS in Statistics, CS, or related field with 0+ years (MS) or BS with 2+ years.
• Practical SAS programming skills.
• Experience with pharmacokinetics and reporting.
• Clear communication skills.

Responsabilidades

• Develop and validate SAS programs for ADaM datasets, Tables, Listings, Figures, and regulatory documentation.
• Consolidate heterogeneous data sources.
• Perform exploratory data analyses and visualizations.
• Collaborate with stakeholders in Statistics, Data Strategy, Medical Writing, and Regulatory Publishing

Conhecimentos

SAS programming

Clinical data analysis

Communication skills

Formação académica

MS in Statistics, Computer Science, or related field

BS with 2+ years of experience

Ferramentas

SAS

Descrição da oferta de emprego

Role: Statistical Programmer supporting clinical research in AbbVie's pharmaceutical R&D, primarily focused on analysis and reporting of clinical trial data.

Responsibilities

• develop and validate SAS programs for creating ADaM datasets, Tables, Listings, Figures, and regulatory documentation
• consolidate heterogeneous data sources
• perform exploratory data analyses and visualizations
• collaborate with stakeholders in Statistics, Data Strategy, Medical Writing, and Regulatory Publishing

Qualifications

• MS in Statistics, Computer Science, or related field with 0+ years (MS) or BS with 2+ years of experience
• practical SAS programming skills
• experience with pharmacokinetics and reporting
• clear communication skills

Preferred

pharma industry experience.

High-Value

role supports drug development, likely in phases involving clinical trial data analysis, with emphasis on regulatory compliance (CDISC standards); cross-functional collaboration across research teams.

WorkSetup

not specified; typically office-based or hybrid.