Job Summary

• You will craft regulatory-grade evidence from real-world data, guiding submissions that can speed approvals, support label expansions, and fulfill post-market commitments.
• Joining our growing epidemiology and real-world evidence capability, you will apply statistical methodologies tailored for registries, align to AstraZeneca standards, and contribute to a portfolio that demands rigor, creativity, and impact.
• Join a company that pairs the energy and autonomy of a pioneering biotech approach with the scale and investment of a global biopharma.

Matching Summary

Skills & Requirements

Key Requirements

• Advanced degree or equivalent experience in statistics, biostatistics, epidemiology
• Hands-on proficiency with R and/or SAS
• Solid understanding of SQL or Python
• Demonstrated experience generating real-world evidence for rare disease programs
• Track record of contributing to regulatory submissions using registry-based analyses

Work Rights