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Current Experience

  • Managing Director
    Since August 2016
    Clinical Data Management Expert, located in the Netherlands. I have extensive experience in helping companies and researchers with clinical data management processes of phase I-IV studies across different therapeutic areas. I provide clinical data management services, thereby following the relevant laws and regulations (e.g. ICH GCP and 21CFR Part 11). The services are delivered in several widely accepted electronic data capture systems.

Past Experience

  • Director Data Management
    December 2015 --- July 2016
    In December 2015 Clinquest was acquired by Accelovance. My job title and corresponding responsibilities remained the same as they were prior to the acquisition.

  • Director Data Management
    June 2009 --- November 2015
    In my role as Director Data Management at Clinquest I was responsible for the supervision of the data management activities for the phase I through phase IV clinical trials. I ensured that the data management team met or exceeded the agreed project timelines. Besides, I served as the primary contact person for sponsors and vendors for all service related issues. I also developed and implemented effective SOPs and was involved in the identification, evaluation and selection of different EDC systems, IWRS systems and ePRO systems.

  • Director Data Management
    July 1998 --- May 2009
    As the Director Data Management I was responsible for setting up the Data Management department at Clinquest Europe and building the data management team. I provided leadership in the delivery of our clinical data management services. Furthermore, I successfully led a system validation team on all aspects of the system validation on Clintrial 4.2, ensuring the system validation was compliant with GAMP4 guidelines.

  • Data Manager
    January 1995 --- January 1998


LinkedIn Assessment :
Clinical trialsEDCGCPCROSOP developmentCRF designLine ManagementClinical DevelopmentBudget ProposalsPharmacovigilanceComputer System ValidationClinical researchClinical monitoringClinical Data ManagementData ManagementQuality AssuranceCTMSCDISConcologyMedDRAOracle ClinicalClinical Study DesignDrug DevelopmentStandard Operating Procedure (SOP)


  • MSc in from Universiteit van Amsterdam in 1995
  • in from Bernrode in 1988

Area / Region

Rosmalen, Netherlands


Driving License
  • Yes