Principal Statistical Programmer

Job Overview:As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies.
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 listingThe programming of analysis datasets (derived datasets) and transfer files for internal and external clientsThe programming quality control checks for the source data and to report the data issues periodicallyAbility 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 teamsFulfil 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 timelinesEstimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverablesUse and promote the use of established standards, SOP and best practicesProvide training and mentoring to SP team membersRequirements:Bachelor's Degree in Maths, Computer science, Statistics, or related field7+ years’ Statistical Programming experience within the Life Science IndustryStrong Efficacy experienceAdvanced knowledge of statistics, programming and/or clinical drug development processAdvanced knowledge of computing applications such as R, SAS, SAS Graph and SAS Macro LanguageAdvanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)Join IQVIA to see where your skills can take youUnleash your potential It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forwardGlobal exposureVariety of therapeutic areasCollaborative and supportive team environmentAccess to cutting-edge and innovative, in-house technologyExcellent career development and progression opportunitiesWork-Life Balance, with a strong focus on a positive well-beingThis role is not eligible for UK visa sponsorshipIQVIA 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.
ComIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.