The role involves planning and coordinating integrated programming solutions for complex clinical studies across the full spectrum of statistical needs
Job Summary
The role involves planning and coordinating integrated programming solutions for complex clinical studies across the full spectrum of statistical needs.
Candidates will provide internal consulting services, interpret project requirements, and act as a technical team lead for single or groups of studies.
IQVIA offers global exposure, excellent career development opportunities, and a strong focus on work-life balance within a supportive team environment.
Matching Summary
The role involves planning and coordinating integrated programming solutions for complex clinical studies across the full spectrum of statistical needs.
Skills & Requirements
Must-have
7+ years Statistical Programming experience
Advanced Base SAS and SAS Macro Language
Strong CDISC ADaM SDTM data standards knowledge
Experience with statistical tables figures listings
Ability to lead complex study projects
Nice-to-have
Training and mentoring capabilities
Collaborative global team environment
Access to cutting-edge in-house technology
Strong communication with statisticians
Interest in therapeutic area variety
Key Requirements
Bachelor's Degree in Maths, Computer Science, Statistics or related field
7+ years' Statistical Programming experience in Life Science Industry
Advanced knowledge of statistics and clinical drug development process