Specifications and Documentation: Write clear programming specifications and oversee completeness of all relevant documentation to support audit-ready deliverables.
Standards and Automation: Ensure adherence to CDISC and internal standards; promote and apply automation to enhance efficiency and consistency across studies.
Continuous Improvement: Contribute to or drive best practices and technical initiatives that elevate quality, speed, and effectiveness within the function.
Risk Management: Identify, manage, and communicate programming risks proactively, maintaining delivery momentum and enabling informed decisions.
Cross-Functional Collaboration: Work closely with statisticians, lead programmers, data managers, and study leaders to align on priorities and resolve issues rapidly.
Vendor Partnership: Collaborate with contract programming providers to ensure outcomes meet AstraZeneca’s standards and business needs.
Stakeholder Influence: Provide subject matter expertise on programming topics, shaping study strategies and decisions.
Project Management: Apply project management principles to plan, track, and deliver programming aspects of drug or technical projects.
Essential Skills/Experience
Degree in Mathematics (i.e., Applied Math, Engineering, etc.), Statistics, Computer Science, Life Science, or equivalent.
Excellent programming skills in SAS (or R) and SAS macros.
Proficient knowledge of the clinical development process and industry standards (CDISC).
Ability to apply programming knowledge to problem solving.
Ability to manage relevant documentation.
Ability to influence relevant stakeholders on Programming related items.
Current knowledge of technical and regulatory requirements relevant to the role.
Desirable Skills/Experience
Broad experience across multiple therapeutic areas and across all phases of clinical trials.
Experience in regulatory submissions and interactions.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Why AstraZeneca: Here, your programming turns raw clinical data into insights that shape trial decisions and submissions, directly impacting patients worldwide. You will work with cutting-edge methods and diverse specialists who challenge assumptions, share knowledge, and support bold ideas—balancing ambition with kindness to help you grow. We prize curiosity and resilience, empowering you to improve processes, learn from setbacks, and contribute visibly across therapy areas. This is a place where evidence matters and your craft can unlock better, faster routes to medicines.
Call to Action: If you’re ready to lead study programming that transforms data into decisive evidence and advances life-changing medicines, take the next step and apply today!
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
