AbbVie

Contribute to design, analysis and reporting of clinical trials or other scientific research studies
Assist with development of protocols and/or statistical analysis plans
Identify and report data issues or violations of study assumptions
Perform statistical analyses as per the analysis plan
Collaborate with Statistical Programming to ensure delivery of high-quality outputs
Develop strategy for data presentation and inference

🎯 Requirements

MS (with 4+ years of experience) or PhD in Statistics, Biostatistics, or a highly related field
Experience with R and SAS
Experience with statistical computations and simulations
Experience with clinical trials statistics (preferred)
Experience based in Oncology (preferred)
High degree of technical competence and effective communication skills

🎁 Benefits

Comprehensive package of benefits including paid time off (vacation, holidays, sick)
Medical/dental/vision insurance and 401(k)
Eligible for short-term incentive programs

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