Offre Emploi CDI Real World Evidence Belgique - Recrutement par Astek

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.

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.