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Clinical Study Coordinator

4 mesi fa

Milano, Italia Ospedale San Raffaele A tempo pieno

L'IRCCS Ospedale San Raffaele, struttura clinica-scientifica-universitaria di rilievo internazionale e di alta specializzazione per diverse importanti patologie, sta ricercando un/a figura di Clinical Study Coordinator da inserire all’interno del Clinical Trial Center - Area Trial StartUp. Si tratta di un’interessante opportunità per inserirsi in un contesto internazionale, dinamico e innovativo, orientato alla crescita professionale e relazionale, con un forte coinvolgimento in progetti sfidanti. Stiamo cercando persone entusiaste, che abbiano un approccio propositivo al lavoro.
**Attività principali**:
revisionare i protocolli/emendamenti sponsorizzati da un punto di vista tecnico scientifico, in sinergia con l’Ufficio Contratti del CTC, per la negoziazione di budget e contratto;
interazione con sponsor/CRO/Sperimentatori/Study Coordinator per l’attivazione di uno studio clinico/emendamento sponsorizzato;
aggiornamento database/portali in uso presso l’Area Sviluppo Protocolli e Regulatory;
gestione ed archiviazione della documentazione.
**Cosa non può mancare**:
Laurea magistrale o a ciclo unico in discipline scientifiche in ambito sanitario (ad esempio biologia, farmacia, CTF);
Certificazione GCP aggiornata;
Esperienza come Study Coordinator di almeno tre anni;
Pregressa esperienza in CRO/Pharma costituisce un plus;
Orientamento al risultato nel rispetto di deadline ben definite;
Buona conoscenza della lingua inglese;
Capacità organizzativa e di problem solving, precisione e attenzione ai dettagli;
Attitudine al team working e ottime capacità comunicative e relazionali.
**Dettagli lavorativi**:
**tipologia contrattuale**: assunzione a tempo determinato;
**Durata**: 12 mesi;
**Sede**: Centro Direzionale Milano 2 - 20054 Milano 2, Segrate (MI).
In IRCCS Ospedale San Raffaele, centro di eccellenza di fama mondiale per le sue attività cliniche e scientifiche, crediamo che considerare la diversità e promuovere un ambiente aperto e inclusivo sia fondamentale per il nostro successo. Ci impegniamo a garantire pari opportunità di lavoro, basate sul merito, senza distinzione di età, religione, sesso, disabilità, condizioni mediche, orientamento sessuale, estrazione culturale e sociale, identità o espressione di genere, origine nazionale o etnica o qualsiasi altro status legalmente riconosciuto che abbia diritto alla protezione in base alle leggi vigenti. Offriamo condizioni stimolanti e riconoscimenti adeguati a un'organizzazione di ricerca competitiva a livello internazionale.