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Summary

With a professional experience of twelve years under my belt in clinical studies, I developed a very good scientific culture especially in oncology.I have been able to acquire organizational skills, autonomy. I also gained an ability to communicate with various stakeholders such as sponsors, investigators, vendors, patients ...

Experiences

Current Experience

  • Clinical Research Associate (CRA) II Wavre, Belgium
    Since April 2015

    Perform processes supporting the conduct and monitoring of a clinical trial in Belgium. Verify that the investigator and the investigator’s site staff are performing the specified trial functions in accordance with the protocol, ICH GCP and any other written agreement between the sponsor and the investigator / institution Check the accuracy or completeness of the CRF entries, source data documents, and other trial-related records against each other

Past Experience

  • Study Coordinator La Louvière, Belgium
    April 2012 --- March 2015

    Coordinates and administers research study associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol, and regulatory requirements are followed. Recruits and coordinates research subjects, as appropriate, and serves as principle administrative liaison for the project. Oversees and coordinates the provision of administrative and staff services to director the investigators; develops and maintains recordkeeping systems and procedures.

  • Site Management (Clinical research associate CRA)
    February 2008 --- April 2012
    Perform processes supporting the conduct and monitoring of a clinical trial in Belgium. Verify that the investigator and the investigator’s site staff are performing the specified trial functions in accordance with the protocol, ICH GCP and any other written agreement between the sponsor and the investigator / institution Check the accuracy or completeness of the CRF entries, source data documents, and other trial-related records against each other

  • Study coordinator
    January 2002 --- January 2008
    Coordinates and administers research study associated activities. Assists in project planning, and ensures that pre-established work scope, study protocol, and regulatory requirements are followed. Recruits and coordinates research subjects, as appropriate, and serves as principle administrative liaison for the project. Oversees and coordinates the provision of administrative and staff services to director the investigators; develops and maintains recordkeeping systems and procedures.

Knowledge

LinkedIn Assessment :
Clinical trialsClinical monitoringICH-GCPCTMSGCPoncologyEDCClinical researchTherapeutic AreasPharmaceutical Industry

Education

  • Bachelor of Science (B.S.) in from Ecole Saint-Exupéry Brazaville in 1992

Training and Certification

  • GCP in 2014 Certification

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
Professional Proficiency
Dutch
Elementary Proficiency

Work Preferences

  • Notice Period:
    12 weeks
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position :    80% FTE
    BrightOwl employee :    80% FTE
  • International:
    Yes

Area / Region

Belgique

Others

Driving License
  • Yes