Senior Statistical Programmer

2 weeks ago


Copenhagen, Copenhagen, Denmark IQVIA Full time

Job Summary


As a Senior Statistical Programmer at IQVIA, you will play a key role in developing process methodologies to meet internal and external clients' needs. You will plan and coordinate the development of integrated programming solutions, serve the full spectrum of statistical programming needs, and provide technical expertise and leadership to the department.


Main Responsibilities



  • Perform, plan, coordinate, and implement the following for complex studies: programming, testing, and documentation of statistical programs; programming of analysis datasets and transfer files; programming quality control checks.
  • Interpret project-level requirements and develop programming specifications as appropriate.
  • Provide advanced technical expertise in conjunction with internal and external clients and independently bring project solutions to SP teams and the Statistical Programming department.
  • Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables.
  • Provide training and mentoring to SP team members.

Requirements



  • 5+ years of Statistical Programming experience within the Life Science industry.
  • BSc or MSc degree in Biostatistics or a related field.
  • Experience in SAS Base and good knowledge of SAS graph and SAS Macros.
  • Ability to implement advanced statistical procedures as per specifications provided by Biostatisticians.
  • Excellent knowledge of CDISC standards (SDTM and ADaM).
  • Thorough understanding of relational database components and theory.
  • Excellent application development skills.
  • Strong understanding of clinical trial data and extremely hands-on in data manipulations, analysis, and reporting of analysis results.
  • Ability to work on multiple projects, plan, organize, and prioritize activities.
  • Experience as a technical team lead directly engaging clients and coordinating tasks within a programming team.
  • In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

About IQVIA


IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. 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.



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