Senior Statistical Programmer

hace 2 semanas

Madrid, Madrid, España IQVIA A tiempo completo
Job Title: Senior Statistical Programmer

At IQVIA, we are seeking a highly skilled Senior Statistical Programmer to join our Global Biostatistics team. As a key member of our team, you will be responsible for providing technical expertise to develop process methodology for the department to meet internal and external clients' needs.

Key Responsibilities:
  • Plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs.
  • Provide technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
  • Perform, plan, coordinate, and implement the following for complex studies:
    • The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing.
    • The programming of analysis datasets (derived datasets) and transfer files for internal and external clients.
    • The programming quality control checks for the source data and report the data issues periodically.
Requirements:
  • 5+ years of Statistical Programming experience within the Life Science industry.
  • BSc or MSc degree in Biostatistics or related field.
  • 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 Biostatistician.
  • 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 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.
What We Offer:
  • 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.

We are 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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