Senior Statistical Programmer II

Job Title: Senior Statistical Programmer II Career Level – D Location: Manyata Tech Park, Bangalore Work Type: Hybrid   Introduction to role: Do you have passion for Programming? Do you consider yourself an SME? Would you like to apply your skills to impact drug development process and regulatory interactions in a company that follows the science and turns ideas into life-enhancing medicines? Then AstraZeneca might be the one for you! Join our 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.   About AstraZeneca: AstraZeneca is a global, science-led, patient-focused pharmaceutical company that focuses on the research, development, and commercialisation of prescription medicines. We aim to transform the lives of patients with improved outcomes and a better quality of life. But we’re more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we 're dedicated to being a Great Place to Work.    Accountabilities: As a Senior Statistical Programmer, you will be working in the Oncology Biometrics Programming department providing statistical programming support and/or leading activities related to the analysis and reporting process at project/study level for the delivery of statistical programming aspects of clinical development. 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.   Essential Skills/Experience: To succeed in this role, you need to be an enthusiastic individual with an understanding of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry. You should have the ability to multitask, collaborate as part of a global team, and have an appetite for solving problems.  Bachelor’s or Master’s (or local equivalent) in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field. At least 3 years of industry experience with Master’s or 5+ years with Bachelor’s  Ability to pay attention to detail and lead/work on concurrent studies and activities Excellent verbal and written communication skills and ability to influence team members Extensive SAS programming expertise to an advanced level within clinical drug development Ability to work independently on the assigned programming tasks Comprehensive knowledge of technical and regulatory requirements Good knowledge of CDISC standards and best of industry practices Experience leading studies or activities in clinical trials Lead experience, Stakeholder management – Oncology TA and Submission experience required   …