Principal Statistical Programmer - FSP (Permanent Homebased)
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, coordinate, and implement the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listings.
Program analysis datasets (derived datasets) and transfer files for internal and external clients.
Conduct programming quality control checks for the source data and report data issues periodically.
Interpret project level requirements and develop programming specifications for complex studies.
Provide advanced technical expertise in conjunction with internal and external clients, independently bringing project solutions to SP teams.
Act as technical team lead for single complex studies or groups 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 timelines for deliverables.
Use and promote 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.
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
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.
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