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Requirements : Experience in clinical research of at least 1 year (0-2 points will be valued: 0.5 pts per year) (certification by a competent body or Responsible Declaration). Experience in statistical
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records and the respective data collection notebooks. – Participate in the selection of patients to be included and management of the patient agenda of the different studies. – Support in statistical
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maximum of 2.5 points). Training related to clinical trials and database management (Good Clinical Practices, SPSS, R statistics). Accredited by certificate issued by a competent body. (They will be awarded
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