Senior Statistical Programmer II

Role Overview

As a Senior Statistical Programmer, you will work in the Oncology Biometrics Programming department providing statistical programming support and/or leading activities related to the analysis and reporting process at project/study level for the delivery of statistical programming aspects of clinical development.

What You Will Do

You will be responsible for clinical study report development, regulatory submissions, commercialization, and the scientific utilization of our data for AstraZeneca products.

Why It Might Be a Fit

You will have the opportunity to work on complex, meaningful problems with a diverse team, and grow through a culture that challenges ideas while celebrating learning.

Requirements

• Bachelor’s or Master’s (or local equivalent) in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field.
• At least 3 years of industry experience with Master’s or 5+ years with Bachelor’s
• Extensive SAS programming expertise to an advanced level within clinical drug development
• Ability to work independently on the assigned programming tasks
• Comprehensive knowledge of technical and regulatory requirements
• Good knowledge of CDISC standards and industry best practices
• Experience leading studies or activities in clinical trials
• Lead experience, Stakeholder management – Oncology TA and Submission experience preferred

Benefits

• Comprehensive knowledge of technical and regulatory requirements
• Good knowledge of CDISC standards and industry best practices
• Experience leading studies or activities in clinical trials
• Lead experience, Stakeholder management – Oncology TA and Submission experience preferred