Bachelor's degree from reputable university preferably in science/ mathematics related fields · Preferred SAS® certification Technical Skills Requirements · Must have expertise of SAS® Base, and good knowledge of SAS® graph and SAS® Macros. · Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician. · Must have excellent knowledge of CDISC standards (SDTM and ADaM) · Thorough understanding of relational database components and theory. · Excellent application development skills. · Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results. · Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes. Experience requirements Minimum of 8+ years of experience in Statistical Programming in pharmaceutical or medical devices industry Desirable requirements · Good verbal and written communication skills. · Ability to work on multiple projects, plan, organize and prioritize activities. Responsibilities At a minimum, following activities are required to be performed; · Perform all responsibilities associated with the Senior Programmer role. · Assist all the Sr. Programmers and Programmers in their day to day activities. · Act as escalation point for Sr. Programmer and Programmer. · Regularly communicates with the sponsor on the progress of programming aspects of the project and proactively anticipates issues and works with the sponsor on resolution of the problems · Provide input and/or write the programming specifications · Serve as subject matter expert on all aspects of SAS programming · Understand pharmaceutical industry standards and trends and proactively plan, develop, and implement · Develop consistent practices of clinical and statistical review of output and mentor programming staff · Check for consistency across therapeutic areas · Identify, plan, and oversee the implementation and success measures of all process improvement initiatives · Maintain expertise in the use of the SAS® Macros and determine macro development priorities · Other responsibilities as defined on ad-hoc basis by senior management. Relationship & Interactions · Clinical data manager · Biostatisticians · Medical Coders IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled