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Moez SHIRI

MALAKOFF

Résultats examens 2026

RETROUVEZ GRATUITEMENT Le résultat du bac à MalakoffLe résultat du brevet à Malakoff

En résumé

Career Objective: To work as a contract clinical research associate (CRA) with a reputed clinical research organization. Performed initiation, study staff training, interim monitoring and close-out visits for multiple sites in accordance with SOPs and the CMP.

Mes compétences :
toxicology
Staff Development and Training
Pharmacovigilance
Immunology
ICH
GCP
Clinical Trials
Administrative monitoring

Entreprises

  • SEEH -  Team Manager

    2014 - 2016 Team Manager : Management of a team (12 employees)

  • Ecobio Laboratory - Research engineer assistant

    2013 - 2013 Research engineer assistant: Selection of the mutants t DNA of the CYP450 involved in the metabolism of PAHs.

  • International Mobility Center - Administrator

    2012 - 2012 Administrator: Administrative monitoring (tender documents, research agreement, contract) for foreign scientists.

  • ENVAM Digital Campus - University teacher

    2012 - 2013 ENVAM Digital Campus, University of Rennes
    Teaching and supervision of Master II students in ecology.

  • Factory Delmotte - Quality Control Laboratory Technician

    2011 - 2011 Factory Delmotte, Broons
    Quality Control Laboratory Technician: Microbiological Sample Control (NPP), Screening Test, Study and Identification of bacterial resistance.

  • INRAP Tunisia and Armand Frappier Institut Qc, Canada - Research engineer

    2008 - 2010 Research project in collaboration between INRAP, Tunis,
    Research engineer: development of a biofilm containing a natural antibacterial agent.

  • hôpital Charles-Nicolle - Internship Laboratory Technician

    2002 - 2005 Laboratory Technician: Immunology, Biochemistry and toxicology.

Formations

  • For Drug Consulting FDC, , France

    Malakoff 2016 - 2016 CRA and PV officer

    Clinical Research:
     Knowledge of the French and European regulatory environment: ANSM, CPP, ARS, CNIL, EMA,” Jardé law and decree of 16 November 2016”.
     Knowledge of GCP, ICH and SOPs.
     Performing documentation and monitoring of all clinical research trial data.
     Updating knowledge of standard protocols for projects.
     Assisting on-site inspection and screening people for clinical trials.
     E

  • University Of Rennes 1

    Rennes 2010 - 2014 PhD in biology

    * Specialty : mechanism involved in the detoxification of Polycyclic Aromatic Hydrocarbon (PAH)
    * Mention: Very honorable with jury congratulations
    * Scientific production: 4 articles with impact factor in peer review
    * International conferences (India, Qc Canada) and 10 national conferences
    * Training (doctoral school VAS, Rennes)
    English research (20)

Réseau

Annuaire des membres :