Medical Affairs Specialist
3 mesi fa
**Informazioni sull’offerta di lavoro**:
Lo.Li. Pharma srl, azienda operante nella commercializzazione di dispositivi medici e integratori alimentari, è impegnata da oltre 20 anni al fianco della classe medica nella ricerca e sviluppo di soluzioni terapeutiche efficaci e innovative con l’obiettivo di supportare la salute delle persone e migliorarne la qualità di vita.
Per ampliamento dell'organico, oggi siamo alla ricerca di un Medical affair specialist al fine di potenziare la ricerca scientifica e le attività editoriali. Il Medical affair specialist sarà parte del dipartimento di ricerca e sviluppo, con i professionisti coinvolti nei progetti, per garantire che la produzione scientifica rispetti gli standard etici e scientifici.
Il Medical affair specialist dovrà essere in grado di comprendere le esigenze dei progetti di ricerca dell'azienda, analizzare i dati provenienti da studi clinici e pre-clinici e redigere testi scientifici di qualità.
**Compiti e responsabilità**
In collaborazione con il Responsabile Ricerca e Sviluppo provvede all’esecuzione delle seguenti attività:
- Redazione e revisione di articoli scientifici in lingua inglese o, occasionalmente, in italiano, e collaborazione alla realizzazione di attività editoriali (numeri speciali, libri,, linee guida, ecc ).
- Gestione dei processi di pubblicazione degli articoli scientifici.
- Stesura di protocolli di studio.
- Organizzazione e/o implementazione di test sperimentali, sia in vitro sia in vivo, e trial clinici a supporto delle attività di ricerca e sviluppo.
- Analisi dei dati ottenuti dalle ricerche sperimentali.
- Supporto scientifico agli altri reparti aziendali, in particolare Medica e Marketing, nella gestione dei prodotti di competenza.
- Collaborazione con il reparto di Medica in merito alla condivisione degli studi scientifici in corso o in fase di progettazione.
- Ricerche bibliografiche sui principi attivi di interesse aziendale e condivisione degli aggiornamenti con le funzioni aziendali.
- Realizzazione di prototipi di prodotto.
- Screening di possibili principi attivi e formulazioni di possibile interesse aziendale.
- Analisi e redazione della sezione técnica di domande di brevetti legati a prodotti delle attività aziendali.
- Redazione della valutazione clinica (compresi gli studi scientifici correlati) da includere nel dossier per la certificazione di Dispositivi Medici, in collaborazione con il dipartimento di Qualità e Regolatorio.
- Mantenimento dei rapporti con gli Opinion Leader.
- Supporto alle attività di Ricerca e Sviluppo (gestione sviluppo di prodotti, gestione progetti)
- Collaborazione con altre funzioni aziendali (in particolare dipartimento Medica, Qualità e Regolatorio e Legale) per quanto concerne lavorazioni legate alle attività di Ricerca e Sviluppo.
**Requisiti necessari**
- Laurea magistrale (o equivalente) in uno dei seguenti settori: scienze biologiche, biotecnologia, medicina, farmacia, chimica, chimica farmaceutica.
- Ottimo livello di inglese scritto e parlato.
**Requisiti preferenziali**
- Dottorato di Ricerca in uno dei seguenti settori: scienze biologiche, biotecnologia, medicina, farmacia, chimica, chimica farmaceutica.
- Esperienza nello sviluppo di Dispositivi Medici e/o AFMS.
- Esperienza di lavoro/studio in paese estero.
Tipologia di lavoro: Tempo pieno in presenza
Orario: Dal lunedì al venerdì dalle 9 alle 18 con flessibilità oraria di 30 minuti.
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