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Summary

i offer: - services in clinical research - as clinical Project Manager, Clinical Research Associate, Clinical Trial manager,... - in pharma, biotech or Medical Device companies or in CRO - start-up and follow-up of Clinical trials/studies according to ich-gcp, iso14155 and regulatory requirements feel free to contact me - by phone on +32 474 26 07 92 - by mail on kathleen@mediprova.be

Experiences

Current Experience

Past Experience

  • Group Lead Internal Operations

    December 2013 --- December 2015

  • Clinical Project Manager (CPM)

    May 2010 --- December 2015

  • Senior Clinical Research Associate (CRA)

    August 2006 --- April 2010

  • Trial Support specialist

    September 2005 --- July 2006

  • Clinical Research Associate (CRA)

    March 2001 --- September 2005

  • Scientific Researcher

    September 1997 --- January 2001

Knowledge

LinkedIn Assessment :
Clinical trialsClinical researchGCPCTMSPharmaceutical IndustryCROClinical DevelopmentMedical DevicesICH-GCPClinical Data ManagementClinical Study DesignoncologyClinical monitoringPolicies & Procedures DevelopmentISOVendor ManagementBudget ManagementTimelinesContract ManagementCoachingClinical StrategyFeasibility StudiesCommunicationRegulatory submissionsElectronic FilingAuditingTeam LeadershipContinuous Process ImprovementmanagementClinical Trial Management System (CTMS)Good Clinical Practice (GCP)CRO management

Education

  • in Course Business Administration from University of Leuven in 2003
  • in Academic Teacher, option Biology from University of Leuven in 1997
  • in Bio-ir in cel-and gene technology from University of Leuven in 1997
  • in from Don Bosco Ruisbroek in 0000
  • in from OLVP in 0000

Area / Region

Belgium

Others

Driving License
  • Yes

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