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Summary

More than 10 years experience in the clinical Research, in which four years as a CRA and four years as a CPM. Experience within pharmaceutical companies as well as CRO, home based and office based. 1 year and 6 months experience in Regulatory Affairs. Specialties:Immunology, oncology, vaccine.

Experiences

Current Experience

  • Clinical Research & Regularory Affairs Consulting-Freelance
    Since January 2014

Past Experience

  • Regulatory Affairs Specialist
    April 2012 --- September 2013
    EU Regulatory Affairs Specialist

  • Clinical Scientist
    January 2010 --- January 2011

Knowledge

LinkedIn Assessment :
Clinical trialsClinical DevelopmentRegulatory submissionsPharmaceutical IndustryRegulatory affairsVaccinesBiochemistryDrug DevelopmentCROImmunologyoncologyClinical researchGCPPharmacovigilanceBiotechnologyLife SciencesSOPGMPCTMSMedical Devices

Education

  • Master's degree in Biochemistry from Université Pierre et Marie Curie (Paris VI) in 2000

Training and Certification

  • cra training in 2002 Certification

Languages

BrightOwl Assessment:
Self Assessment:
English
Full Proficiency
French
Native

Area / Region

Brussels, Belgium

Others

Driving License
  • Yes