As Biostatistician your responsibilities would be:

  • Preparing Statistical Analysis Plans
  • Provide statistical programming support and validation of analysis datasets and statistical analyses
  • Program analysis datasets, pooled datasets, listings, tables, summaries and graphs for clinical trials
  • Provide input in design of databases and analysis
  • Conducting statistical analyses and performing quality control.
  • Perform other duties related to the work described above

Your Profile:

  • Master or PhD in biostatistics, statistics or mathematics.
  • Minimum of 2 years biotech/pharmaceutical/CRO experience
  • Experience with SAS programming is required (knowledge of R would be an asset)
  • Understanding of clinical trial practices, procedures and methodologies
  • Strong computer and analytical skills
  • Good written and verbal communication skills
  • Fluent English
  • Ability to set priorities and respect tight deadlines
  • Problem solving skills, team player

Please send your CV and cover letter in English to IDDI by e-mail: (for Belgium) or (for the US)