LOCATION: Barcelona office (3 days office – 2 working from home)About CVRMAt AstraZeneca CVRM Biometrics we work on a wide range of agile and innovative projects within the Cardiovascular, Renal and Metabolism therapeutic area, providing solutions and treatments for millions of patients across the globe.About the RoleWe are now looking for an experienced and highly motivated individual to join our CVRM team as a Statistical Programmer I, where you will be primarily responsible for data analysis and programming deliverables on a range of drug development projects. Depending on the level of experience, this role may work under the general direction and support of an experienced programmer and require you to collaborate and work alongside a team of statisticians, programmers, data managers, and other stakeholders.Accountabilities:As a Statistical Programmer, you are responsible for contributing to or leading programming deliverables of a clinical study or a small to medium sized clinical project.Provides SDTM, ADaM, TFLs technical programming and information components of a project under required supervision.Understands the contents of protocols and clinical development plans to understand contribution of their work.Works within established frameworks and ensures high quality is built into own deliverables.Works independently for a well-defined scope of work.Continues to acquire knowledge of the drug development process.Continues to increase knowledge of SAS and of the industry standards.Proactively keeps the lead programmer updated on progress of deliveries.Education, Qualifications, Skills, and Experience:Degree in Mathematics (i.e., Applied Math, Engineering, etc.), Statistics, Computer Science, Life Science, or equivalent.Intermediate programming skills in SAS and SAS macros.Relevant Industry knowledge on statistical programming and industry standards (CDISC).Good interpersonal skills and ability to apply programming knowledge to problem solving.Desirable Skills/Experience:Broad experience across multiple therapeutic areas and across all phases of clinical trials.Experience in regulatory submissions and interactions.R or Python programming knowledge is beneficial.At AstraZeneca, we believe in the potential of our people, and you'll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us. As a Statistical Programmer, you'll play a pivotal role in making a positive impact on changing patients' lives.Date Posted: 24-oct-2024Closing Date: 30-dic-2024AstraZeneca 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.
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