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Real World Evidence H/F Astek

  • Belgique
  • CDI
  • Télétravail partiel
  • Bac +5
  • Secteur informatique • ESN
  • Exp. 5 ans min.
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Les missions du poste

Your mission (should you decide to accept it):

Your potential challenges will be various, depending on the clients' priorities. The list below gives you examples of our classic activities.

Your daily activities will be:

  • Support Statistical programming activities in Real World Evidence.
  • Provide input on study design and analysis plans where necessary.
  • Review the study concept, protocol design, analysis plans and other study-related documents.
  • Evaluate the quality of the database.
  • Develop, validate, maintain, and document analysis programs, tables, charts and associated metadata following standard working practices.
  • Ensure that statistical outputs are produced in an efficient manner.

Le profil recherché

You:

  • 5+ years experience in SAS programming.

  • 2+ years experience in Real World Evidence, Epidemiology, or Health Outcomes environment.
  • 2+ years experience with large health care databases such as Clinical Practice Research Database (CPRD) or IBM MarketScan.
  • Advanced statistical programming skills in SAS to solve complex programming tasks.
  • Good study design and epidemiological/statistical analysis experience, including understanding of drug development, observational and epidemiological endpoints and assessments.
  • Knowledge of matching algorithms such as propensity score matching is a plus.
  • Knowledge of R is a plus.

Publiée le 23/05/2026 - Réf : 4886

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