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Experiences

Past Experience

  • Free-lance Senior CRA

    April 2015 --- December 2015
    free-lance senior CRA at. icon plc monitoring, transition and close out of site for phases ii and Phase III studies in oncology

  • Senior Clinical Research Associate (CRA)

    June 2013 --- June 2015
    · participates in the Investigator recruitment process. performs initial Qualification visits of potential investigators. evaluates the capability of the site to successfully manage and conduct the clinical study, both clinically and technically. · works with the study start-up group to coordinate activities with the site in preparation for the initiation of studies. obtains regulatory Documentation for successful implementation, monitoring, and evaluation of Clinical trials. works with study start-up group and site staff to obtain regulatory (irb/iec) approval of study specific documents. · work with the sites concerning study fees and overcoats Negotiation. - monitoring activities

  • Free LanceSenoir CRA

    May 2013 --- March 2014

  • Free lance Senior CRA

    July 2012 --- April 2013
    senior CRA for a phase 1 Neurology study monitoring activities.

  • Free lance Senior CRA

    June 2011 --- February 2012
    monitoring activities ,and close out visits for oncology, knee implants and multiple sclerosis studies

  • Free lance Senior CRA

    May 2009 --- October 2011
    monitoring activities for a prostate Cancer Phase III study

  • Senior clnical consultant

    January 2009 --- January 2010

  • Free lance Senior CRA

    January 2008 --- January 2009

  • Clinical Research Associate (CRA)

    January 1997 --- January 1999

Knowledge

LinkedIn Assessment :
Clinical monitoringInformProstate CanceroncologyGCPBreast CancerClinical trialsOphthalmologyHematologyInfectious diseasesSOPVaccinesPediatricsRheumatologyFDAIRBNeurologyAsthmaEDCGastroenterologyEndocrinologyQueryPharmaceuticalsTherapeutic AreasCROClinical researchRegulatory submissionsICH-GCPTherapeutic AreasSOPPharmaceutical IndustryClinical operationsPharmacovigilanceClinical Data ManagementClinical DevelopmentMedical writingRegulatory affairsMedical affairsProtocolCTMS

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
Full Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA) Clinical Research Consultant Clinical Trial Coordinator (CTC)
  • Locations I am interested in:
    France
  • Work From Home:
    Yes, 0 to 4 days per week
  • Work Regime:
    BrightOwl freelancer :    35 Hours per week :    80% Free Per Month(in coming months)
  • International:
    Yes

Area / Region

Paris, France

Others

Driving License
  • Yes

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