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Senior Statistical Programmer - GRIDDS (Home-Based, Europe & UK)

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Primary Location: Reading, Berkshire, United Kingdom Additonal Locations: Amsterdam, Netherlands,NLD; Antwerp, Belgium,BEL; Barcelona, Spain,ESP; Copenhagen, Denmark,DNK; Frankfurt, Germany,DEU; Milan, Italy,ITA; Solna, Sweden,SWE; Vienna, Austria,AUT; Warsaw, Poland,POL Full time R1211541

Job description

Senior Statistical Programmer - GRIDDS

Home-Based - UK/Europe

Join us on our exciting journey!

From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.

We have one of the largest Biostatistics departments within the industry of around 1,100+ staff. Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.

Job Overview:

The GRIDDS (Graphical Review Interface for Dynamic Data Services) Lead is responsible for coordinating programming activities for graphical data visualization through tools such as JReview and Spotfire in addition to SAS.

This is a client facing role that gives the opportunity to work with a variety of functions and client groups within the organization.

As a Senior Statistical Programmer, you will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients’ needs.

You will plan and coordinate the development of integrated programming solutions, serving data visualization needs and provide technical expertise and leadership to the department and provide consulting services, including specifications and user needs analysis for project or client requirements.

Requirements:

  • Bachelors or Masters’ in Computer Science, Mathematics or equivalent

  • Knowledge of programming and/or clinical drug development process 

  • 5+ years’ experience as technical team lead, directly engaging clients, within the Life-Science industry

  • Ability to work on and lead multiple projects

  • In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines 

  • Working knowledge of Base SAS, SAS/STAT and SAS Macro Language

JOIN US

Embrace your curiosity and grow your career in an exciting environment where development is a priority.

Think boldly and disrupt conventional thinking.

Enjoy what you do.

Whatever your career goals, we are here to ensure you get there!

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

Apply now

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