Statistical Programmer 2 – Global BIOS

Statistical Programmer 2Global BiostatisticsHome-Based/Hybrid: EMEA & UKJoin us on our exciting journey!The Global Biostatistics (Data Sciences, Safety & Regulatory) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.Due to continued growth, we are seeking new brave minds to join our award winning and innovative department. You will have the opportunity to work globally and across a variety of therapeutic areas.IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.Job Overview:As a Statistical Programmer 2, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose.You will also provide advanced technical expertise to develop and maintain programs to meet internal and external clients��� needs.You will plan and lead the development of project-related solutions to the full scope of statistical programming tasks.As a lead programmer on assigned studies, you will write and maintain programming specifications datasets and program TLFs, to maximize programming efficiency with the use of biostatistical tools and assist in training and mentoring new or junior team membersRequirements: Bachelors or Masters��� in Computer Science, Mathematics or equivalent3+ years, statistical programming experience within the Life Science industryExperience as project lead, directly engaging clients and coordinating tasks within a programming teamKnowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesKnowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro LanguageAbility to independently lead multiple tasks and projectsFrom camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.What is in it for you?Global exposureVariety of therapeutic areasCollaborative and supportive team environmentAccess to cutting-edge in-house technologyExcellent career development and progression opportunitiesWork-Life BalanceJOIN USEmbrace your curiosity and grow your career in an exciting environment where development is a priority.Think boldly and disrupt conventional thinking.Enjoy what you do.Whatever your career goals, we are here to ensure you get there!At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible ��� to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.