Clinical Research Specialist

5 giorni fa

Rozzano, Italia Humanitas A tempo pieno

Siamo alla ricerca di una figura che si occupi della gestione autorizzativa delle sperimentazioni cliniche non profit. La figura si interfaccerà con le funzioni interne interessate (ad es. legale, amministrazione, personale medico, farmacia e comitato etico) e si occuperà di:

- Supportare i medici/ricercatori nel disegno di protocolli, in termini di metodologia e obiettivi;
- Garantire la coerenza tra e-crf ed il protocollo;
- Gestire il percorso di istruttoria degli studi;
- Finalizzare il budget degli studi con grant o supporto pharma e le convenzioni con parti terze (supporter/CRO/promotore).

Profilo:
Buona conoscenza della lingua inglese, forte interesse per il settore sanitario e la ricerca clinica, capacità di relazionarsi con le diverse funzioni aziendali, mediche e non; buona capacità di lavorare in team; organizzazione, precisione, problem solving completano il profilo.

Esperienze pregresse nell’ambito della ricerca clinica costituiscono elemento necessario.

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