Clinical Trial Statistical Programmer

5 days ago


Espoo, Uusimaa, Finland IQVIA Full time

IQVIA is seeking a skilled statistical programmer to join our team. As a senior statistical programmer, you will be responsible for utilizing the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions.

Key Responsibilities:
  1. Develop programming specifications based on project level requirements
  2. Program SDTM and ADaM datasets, create statistical analysis tables, listing, and figures
  3. Validate datasets and all statistical outputs per prescribed gate checks
  4. Communicate with internal and client statisticians and clinical team members

This role offers the opportunity to work on global projects across therapeutic areas, bringing clinical trial statistical analysis into the next generation. Our team is collaborative and fast-paced, performing biostatistical analyses and advanced statistical programming.

Requirements:
  • Mastery of SAS programming language and experience working with ADaM/SDTM/TLFs
  • Strong educational or practical background in Biostatistics, Statistics, Mathematics, or Computer Science
  • Excellent accuracy, attention to detail, problem-solving, organizational, and interpersonal communication skills


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