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.Job DescriptionStatistical SAS Programming – Senior SAS Programmer and Associate Director Opportunities Do you have expertise in, and passion for, Programming? Would you like to apply your skills to impact all phases of drug development and regulatory interactions, in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you About AstraZeneca AstraZeneca is a global, science-led, patient-centric biopharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. Join the team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. With multiple indications and high-quality molecules in all stages of our innovative pipeline, we keep pushing forward to conquer cancer through data, innovation and evidence-based decisions. What you'll do You will be working in the Biometrics Programming department providing statistical programming support and leadership on analysis and reporting of our clinical trials. The scope of work includes, but is not limited to, clinical study report development, regulatory submissions, commercialization, and the scientific utilization of our data for AstraZeneca products. There are many career options that you can pursue for your development and progression. We have positions available at both the Senior Programmer (SP) and Associate Director (AD) levels. Responsibilities - Reporting to a Director within the Oncology Programming group you will provide programming expertise in one or more of the following areas: · Lead (AD) or contribute (SP) to the delivery of the Clinical Study Report (CSR), Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases and Tables, Figures and Listings (TFL) outputs through both internal and external delivery models, following applicable data standards and regulations · Lead (AD) or contribute (SP) to the statistical programming deliverables for regulatory submissions, including specification and delivery of pooled safety/efficacy databases, outputs and response to regulatory questions, commercialisation and reimbursements · Lead (AD) or contribute (SP) to the development of standard process to improve quality, efficiency and effectiveness of the Oncology Programming group · Lead (AD) or contribute (SP) to Development Safety Update Reports (DSUR), Periodic Benefit-Risk Evaluation Report (PBRER) and Investigators brochures (IB) Essential for the role: To succeed in this role, you'll be an enthusiastic individual with an understanding of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You'll enjoy multitasking, collaborating as part of a distributed team, and have an appetite for solving problems. You will be an effective communicator, with a strong team focus who enjoys collaborating to achieve the best results. Desirable experience includes: · BSc in a Mathematical (i.E
