Au terme de la formation, les participants devront être capables de concevoir et de mettre en œuvre un protocole de recherche clinique en prenant en compte l’hypothèse de recherche, les résultats attendus du point de vue clinique, les contraintes méthodologiques et la faisabilité du protocole. Les objectifs sont donc de :
● Valider une hypothèse de recherche clinique ;
● Connaître les bases méthodologiques de l’analyse des stratégies médicales diagnostiques, thérapeutiques, curatives et préventives ;
● Analyser des données bibliographiques ;
● Conduire un projet de recherche.
Compétences développées
/
Débouchés
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Organisation de la formation
120 heures d’enseignement réparties en :
● 40 heures : séminaire d’une semaine en décembre
● 40 heures : session d’une à deux journées
● 40 heures : mémoire (travail personnel dirigé par un tuteur)
Un tuteur aura au maximum 3 étudiants.
Contrôle de connaissances
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Condition admission / Public cible
● Docteurs en pharmacie, en médecine ou en odontologie ainsi que les étudiants en cours de 3ème cycle de ces filières ;
● Sages-Femmes, vétérinaires et paramédicaux diplômés ;
● Les titulaires d’un D. U. de niveau maîtrise minimum.
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