IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services, including consulting services. It has a network of more than 58,000 employees in more than 100 countries.As of 2017, IQVIA was reported to be one of the world's largest contract research organizations This involves planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs. You will provide internal consulting services, including specifications and user needs analysis for complex project or client requirements. Key Responsibilities: Perform, plan co-ordinate, and implement the following for complex studies: The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing The programming of analysis datasets (derived datasets) and transfer files for internal and external clients The programming quality control checks for the source data and to report the data issues periodically Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies. Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies. Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables Use and promote the use of established standards, SOP and best practices • Provide training and mentoring to SP team members Requirements: Bachelor's Degree in Maths, Computer science, Statistics, or related field 7+ years’ Statistical Programming experience within the Life Science Industry Strong Efficacy experience Advanced knowledge of statistics, programming and/or clinical drug development process Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM) Join IQVIA to see where your skills can take you Global exposure Variety of therapeutic areas Collaborative and supportive team environment Access to cutting-edge and innovative, in-house technology Excellent career development and progression opportunities Work-Life Balance, with a strong focus on a positive well-being