Gigg från: Astrazeneca AB
Do you have expertise in, and passion for, Statistical 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 Astra Zeneca might be the one for you! Astra Zeneca is a global, innovation-driven Bio Pharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious disease. Working as part of Data Science and AI, you'll be able to access technology at the forefront of science in an innovative environment, where you will have scope to develop creative statistical ideas and approaches, and to apply them in your work. At Astra Zeneca we're driving leading-edge approaches to drug development across many business areas - within Early Biometrics & Statistical Innovation (EB&SI) a data-centric focus is helping us work more efficiently and creatively to bring the right medicines to the right patients. Our biometrics teams use their expertise in statistics and programming to answer drug development objectives and reduce uncertainty in product development, driving better business decisions with quantitative reasoning. We work on some of the most complex and interesting challenges. A fast-paced and agile team, we are empowered and trusted to innovate and experiment. With access to our extensive capabilities and comprehensive pipeline, you'll be involved in countless submissions and a wide range of engaging projects along the complete drug development process. The Senior/Principal Programmer sits within our Early Programming group in EB&SI, aligned either to Cardiovascular/ Renal/ Metabolism (CVRM) or Respiratory, Inflammation, and Autoimmunity (R&I), and is responsible for providing statistical programming expertise to support the design and interpretation of early clinical studies and development programmes. In this role, we will give you the chance to utilise your statistical programming expertise in analysis and reporting of clinical trial programs; submission and defence of regulatory filings and the generation of evidence to support product commercialisation and reimbursement. What you'll do The Senior/Principal Programmer provide Statistical Programming support and/or lead all programming related activities of the analysis and reporting process including, but not limited to, CSR development, regulatory activities and the scientific utilization of our data for Astra Zeneca products. There are many career options you can pursue for progression including technical pathways, management of global projects or line management. You will work in the Programming department that not only oversees and delivers the programming aspects of analysis and reporting but also manages and maintains our end-to-end standards and our analysis and reporting production tools. You'll be part of a global team that pulls together to put patients first. Essential for the role To succeed in this role, you'll be an experienced programmer with good knowledge of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You'll enjoy multitasking, have an appetite for solving problems with a strong team focus who enjoys collaborating to achieve the best results. We have several opportunities across both Senior and Principal levels. Desirable experience includes: Both * BSc in a Mathematical (i.e. Applied Math, Engineering, etc.), Statistical, Computer Science or Life Science subject * Excellent problem-solving skills * Diligence - attention to detail and ability to manage concurrent projects and activities * Excellent verbal and written communication skills and ability to influence stakeholders Senior * SAS programming expertise gained within a clinical drug development or healthcare setting * Knowledge of CDISC standards and industry best practices * Knowledge of database set-up and report publishing requirements Principal * Extensive SAS programming expertise to an advanced level * Extensive Knowledge of Analysis and Reporting within Clinical Development * Comprehensive knowledge of technical and regulatory requirements with submission experience * Wide-ranging knowledge of CDISC standards and industry best practices * Travel - willingness and ability to travel domestically and/or internationally * Team centric approach: keen to take steps to understand and appreciate the roles, skills and strengths of others on the team Join the team unlocking the power of what science can do. We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Why Astra Zeneca? At Astra Zeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare. So, what's next? Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it's yours. Welcome to apply no later than 17th of April, 2021. Location: Gothenburg Competitive salary and benefits Closing Date 16-Apr-2021
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