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more than 15 years experience in clinical research and development of which 10 years in pharma and 5 years in Vaccines development. walked all the levels in Career development from Clinical Research Associate up to Director in Project Management. currently, managing global projects in Vaccines development. success factors: taking Leadership in day to day business, driving people into making decisions, focusing on open and clear Communication channels and delivering study results with high quality. highly visible personal knowledge and skills in day to day Project Management resulting into high commitment, motivation and passion for work.


Current Experience

  • Director Clinical Project Management

    Enter Location
    Since April 2009

    currently, managing a  vaccine project involving budget, timelines, quality and study Risk Assessment. used to work with the tools in Clinical Project Management: ms plan, cost management plan, study risk register, issue escalation register, Communication management plan, Quality Management plan.

    Currently, managing a  vaccine project involving budget, timelines, quality and study risk assessment. Used to work with the tools in clinical project management: MS plan, cost management plan, study risk register, issue escalation register, communication management plan, quality management plan.

Past Experience

  • Clinical Research Manager Pharma

    June 2003 --- April 2009

  • Senior Clinical Research Associate (CRA)

    September 2001 --- September 2003


Self Assessment :
AssertivenessCompetitivenessAttention to detailProblem solvingResponsibilityService orientedResult OrientedResiliencyProactivity


Self Assessment :
VaccinesStudy protocolsProject Management
LinkedIn Assessment :
GCPCROClinical trialsICH-GCPPharmaceutical IndustryVaccinesClinical researchCTMSClinical monitoringClinical Development

Skills and Expertise

Self Assessment :
Administer, maintain and co-ordinate the logistical aspects of clinical trialsWork cross-functionallyWork collaboratively with the other members of the clinical research team Train StaffTeachingSet up a clinical studySelect contractors Select investigators


  • Master's degree in Biomedical science in from Vrije Universiteit Brussel in 2005

Training and Certification

  • ICH-GCP training in 2015 Certification
  • Project management for professionals in 2014 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Notice Period:
    9 weeks
  • Positions I am interested in:
    Clinical Operations Manager Clinical Project Manager (CPM) Clinical Project Leader Clinical Research Consultant Clinical Research Manager Clinical Trial Manager (CTM) Clinical Trial Specialist (CTS)
  • Locations I am interested in:
  • Work From Home:
    Yes, 3 to 5 days per week
  • Work Regime:
    Permanent position :    80-90% FTE
    BrightOwl freelancer :    32 Hours per week
  • International:

Area / Region

Gent, Belgium


Driving License
  • Yes

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