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.Responsibilities

Perform, plan, co-ordinate, and implement programming activities for complex studies, including programming, testing, and documentation of statistical programs used to create statistical tables, figures, and listings.Program analysis datasets (derived datasets) and transfer files for internal and external clients.Conduct programming quality control checks on source data and report data issues periodically.Interpret project-level requirements and develop programming specifications for complex studies as appropriate.Provide advanced technical expertise in collaboration 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 a group of studies.Directly communicate with internal and client statisticians and clinical team members to ensure understanding of requirements and project timelines.Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate timelines for deliverables.Use and promote established standards, SOPs 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.Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM).Benefits

Global 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-beingIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

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