Senior Statistical Programmer: Iqvia Biotech – homebased or hybrid working

  • Full time
  • Prague
  • Posted 2 months ago

Join us on our exciting journey!

Innovative emerging biopharma and biotech companies are driving the drug development pipeline; competition for funding and resources is fierce. IQVIA Biotech delivers flexible clinical development solutions designed for the specific needs of such biotech companies. We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities!

Job Overview:

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 the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

Acting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and support the training of new or junior team members. As well as estimating programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.

Please apply in English

Essential Requirements:

  • 5+ years Statistical Programming experience within the Life-Science industry
  • Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros
  • Ability to implement more advanced statistical procedures as per specifications provided by Biostatisticians.
  • Excellent knowledge of CDISC standards (SDTM and ADaM)
  • Already possess the right to work in EMEA
  • Thorough understanding of relational database components and theory
  • Excellent application development skills
  • Experience as technical team lead, directly engaging clients and coordinating tasks within a programming team
  • Bachelors or Masters’ in Computer Science, Mathematics or equivalent
  • In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice
  • (GCP) and International Conference on Harmonization (ICH) guidelines

    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!


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