Location: Homebased anywhere in the USnnPurpose:nnJoin our FSP team today! In this role you will plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.nnJob Details:nnPosition: – Principal Statistical ProgrammernnHome BasednnMin 4+ years of CRO/Pharma IndustrynnTherapeutic Areas: Oncology // Immunology // IDV // EDCPnnKey Skills:nnMust have expertise of R programming as well as SAS® Base, and good knowledge of SAS® graph and SAS® Macros.nnCapable of implementing more advanced statistical procedures as per specifications provided by biostatistician.nnMust have excellent knowledge of CDISC standards (SDTM and ADaM)nnThorough understanding of relational database components and theory.nnExcellent application development skills.nnStrong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.nnGood understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes.nnMinimum of 4+ years of experience in Statistical Programming in pharmaceutical or medical devices industrynnGood verbal and written communication skills.nnAbility to work on multiple projects, plan, organize and prioritize activities.nnRequired Knowledge, Skills and Abilities:nnExperience as technical team lead directly engaging clients and coordinating tasks within a programming teamnnIn-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesnnKnowledge of statistics, programming and/or clinical drug development processnnAdvanced knowledge of R programmingnnBase SAS, SAS/STAT, SAS Graph and SAS Macro LanguagennShould have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.nnMust have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL.nnGood organizational, interpersonal, leadership and communication skillsnnAbility to independently manage multiple tasks and projectsnnAbility to delegate work to other members of the SP teamnnExcellent accuracy and attention to detailnnAbility to delegate work to other members of the SP team (SPM)nnExhibits routine and occasionally complex problem-solving skillsnnAbility to lead teams and projects and capable of managing at a group levelnnRecognizes when negotiating skills are needed and seeks assistance.nnAbility to establish and maintain effective working relationships with co-workers, managers and clients.nnResponsibilities:nnPerform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically..nnAbility to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.nnProvide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.nnFulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.nnDirectly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.nnEstimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.nnUse and promote the use of established standards, SOP and best practices.nnProvide training and mentoring to SP team members and Statistical Programming department staff.nnMINIMUM REQUIRED EDUCATION AND EXPERIENCE:nnBachelor's degree from reputable university preferably in science/ mathematics related fieldsnnIQVIA 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 are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. potential base pay range for this role, when annualized, is $117,400.00 - $218,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.nnIQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.nnTo get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.nnEEO Minorities/Females/Protected Veterans/Disabled