Statistical programmer 2
IQVIA Holdings Inc.
Copenhagen Ø, Denmark
Statistical Programmer 2
Real World Evidence
Home-based, office-based, hybrid options available
The vision of our Real World Evidence teams is to pioneer and lead with scientific and technical expertise, the generation and dissemination of high-quality Real World Evidence that make a true difference to patient lives, globally. Come join us on this exciting journey!
Our Real World Global Biostatistics & Statistical Programming team delivers insightful analytics for predominantly primary data collection studies, and we are increasingly supporting innovative studies such as External Comparators, Enriched Studies, and Pragmatic Trials.
We are a highly motivated global team of more than 150 employees, responsible for engaging with our clients early to help shape the statistical analysis in these various study designs; contribute to protocols and deliver results that meet their needs.
We have unique opportunities to define the way our clients develop and apply Real World Evidence for healthcare decision making, so we are looking for the best talent to join us in this effort.
We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of Real World Evidence in an evolving industry!
Job Overview:
As a Statistical Programmer 2, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.
You will also provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs.
You will plan and lead the development of project-related solutions to the full scope of statistical programming tasks.
As a lead programmer on assigned studies, you will write and maintain programming specifications datasets and program TLFs, to maximize programming efficiency with the use of biostatistical tools and assist in training and mentoring new or junior team members
Requirements:
Bachelors or Masters’ in Computer Science, Mathematics or equivalent
3+ years, statistical programming experience within the Life Science industry
Experience as project lead, directly engaging clients and coordinating tasks within a programming team
Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language
Ability to independently lead multiple tasks and projects
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
Unleash 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 forward.
Job posted: 2023-10-18
