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ASSOMONITOR is the Italian Society of Clinical Monitors that collects and represents both freelancer and employed CRA’s (Clinical Research Associate), working in pharmaceutical companies and CROs (Contract Research Organizations).

Assomonitor is affiliated with CNA Professioni to guarantee the highest and common professional  standard of CRA’s, with respect to the general requirements of quality of each subject involved, with various qualifications, in the field of Clinical Research and every kind of effort will be invest to achieve legislative and fiscal classification of Italian Clinical Monitors.

The Association promotes free of payment trainings on this website, in compliance with Ministerial Decree of 15 November 2011, “Definition of the minimum requirements which Contract Research Organisations (CRO) shall satisfy in order to work within clinical trials on medicinal products”, and other services, free of payment too, only reserved for the associates of Assomonitor.

Assomonitor guarantees the validity of training certificates incurred by its associates, enabling CRO and Pharmaceutical Companies to verify their actual achievement for the purposes of DM 15 Nov 2011.

News

(click on titles for links)

Pamplona Capital to Take Parexel Private for $4.5 Billion 21/06/2017 U.S. pharmaceutical research services provider Parexel International Corp said on Tuesday it would be taken private by Pamplona Capital Management LLP in a $4.5 billion deal. For further details http://www.reuters.com/article/us-parexel-intl-m-a-pamplona-idUSKBN19B0XT

New Directive Council elected 21/06/2017 Assomonitor has a New Directive Council elected during the last annual meeting held in Rome on June 17, 2017. Please refer to the dedicated area for details.

Requisiti per svolgere l'attività di Clinical Monitor

  • possesso del diploma di laurea in discipline sanitarie/
    scientifiche attinenti alle tematiche da svolgere;

  • almeno 40 ore di formazione teorica effettuata
    nell’arco dei 12 mesi che precedono l’inizio delle attività
    di monitoraggio in relazione ai seguenti argomenti:
    1) metodologia e normativa della sperimentazione
    clinica;
    2) GCP;
    3) norme di Buona Pratica di Fabbricazione (GMP)
    con specifico riferimento al farmaco in sperimentazione;
    4) farmacovigilanza;
    5) sistemi di qualità e assicurazione di qualità;
    6) compiti del monitor di cui al paragrafo 5.18
    dell’allegato 1 al decreto ministeriale 15 luglio 1997

  • almeno 20 giorni di attività di monitoraggio in
    affiancamento a monitor esperti effettuati nei 12 mesi
    precedenti l’inizio dell’attività autonoma di monitoraggio.

 
 
 

 

Principali servizi offerti ai soci (inclusi nella quota associativa):

  • Training online (certificato rilasciato immediatamente e archivio dei training frequentati)

  • Newsletters

  • Accesso alle offerte di lavoro (e loro ricezione sulle caselle di posta dei soci)

  • Casella di posta con dominio @assomonitor.org

  • Casella di posta certificata con dominio @pec.assomonitor.org

  • Consultazione della lista dei soci

  • Download delle ricevute di pagamento

 

 

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