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successful launch and support: - Gynecology : hormone replacement therapy + hormone loaded intra-uterine device + prostaglandins - uro-Gynecology : Treatment for unstable bladder - onco-Gynecology : adjuvant hormonal therapy for breast Cancer - endocrine care : antidiabetic Treatment + pituitary Treatment + growth hormone - Critical Care : antibiotics + antifungals + corticosteroids intensive scientific collaboration with key opinion leaders in different specialism’s : Microbiology, intensive care, Infectious diseases, anesthesiology, Intern Medicine (pneumology/ Endocrinology/ Hematology/ oncology), Surgery, Pediatrics, Gynecology detected needs in the field and initiated projects to the medical department in the Critical Care area. participation as representative in development of Sales strategies thanks to a strong scientific product knowledge participation as representative in the Translation and implementation of product information into Sales skills


Current Experience

  • Clinical Research Associate (CRA)

    Since September 2012
    Clinical Research Associate aephis Consulting - responsable for study initiation (4 centers in belgium)-Phase II study (Gastroenterology) for a CRO (site initiation) - responsible for study monitoring (4 centers in belgium)-Medical Device study (Dermatology) for a CRO (site initiation/site monitoring/site management) - responsible for survey monitoring (3 centers in belgium/1 center in the netherlands)- neonatology for a CRO (site initiation/site monitoring/site management)-ongoing - allround support for a Pharmaceutical company (submission/file review/translations/organization) - responsible for study monitoring (12 centers in belgium) Phase IV study (Cardiology) for a CRO (pre-study/site initiation/site monitoring/site close out/site management) Clinical Research Associate Aephis Consulting - Responsable for study initiation (4 centers in Belgium)-Phase II study (Gastroenterology) for a CRO (Site initiation) - Responsible for study monitoring (4 centers in Belgium)-Medical Device study (Dermatology) for a CRO (Site Initiation/Site Monitoring/Site management) - Responsible for survey monitoring (3 centers in Belgium/1 center in The Netherlands)- Neonatology for a CRO (Site Initiation/Site Monitoring/Site management)-ongoing - Allround support for a pharmaceutical company (Submission/File Review/Translations/Organization) - Responsible for study monitoring (12 centers in Belgium) Phase IV study (Cardiology) for a CRO (Pre-study/Site initiation/Site monitoring/Site close out/Site management)

Past Experience

  • Senior Critical Care Specialist

    January 2003 --- January 2012
    antibiotics/ antifungals/ corticosteroids focus on intensive care, Hematology, Infectious diseases, Intern Medicine, Surgery, Microbiology, anesthesiology, Hospital Pharmacy

  • Medical Sales Representative

    January 2001 --- January 2003
    Gynecology/endocrine care focus on hormonal substitution therapy for menopause and pituitary gland/ adjuvant hormonal therapy for breast Cancer/ Treatment for overactive bladder

  • Medical Sales Representative

    January 1996 --- January 2001
    Gynecology/ endocrine care/ stomatology/ Dermatology

  • Medical Sales Representative

    January 1994 --- January 1996
    generalists/ Gynecology/ endocrine care

  • Medical Sales Representative

    January 1987 --- January 1994
    generalists/ Gynecology/ endocrine care


Self Assessment :
Attention to detailCommunicativeFlexibilityProactivityProblem solvingResponsibilitySelf-disciplineTrust


LinkedIn Assessment :
OB/GYNPulmonologyEndocrinologyAnti-infectivesDiabetesPharmaceutical salesHematologyOrthopedicsInfectious diseasesBacterial CultureAntibioticsClinical Research Training for Junior CRAs. ECCRT BrusselsCommunication SkillsTime ManagementInfectionPharmaceutical IndustryMedical DevicesOrthopedicTrainingAntibacterialGynecologyHospital SalesSurgeryICH GCP Refresher


  • University in Physical Education and Biology from Katholieke Universiteit Leuven in 1984
  • High School in Wetenschappelijke B from Sint-Andreaslyceum Brugge in 1980

Training and Certification

  • ICH-GCP Training (ECCRT, Brussels) in 2015 Certification
  • European Legislation for Clinical Research-Implementation in Belgium (ECCRT,Brussels) in 2014 Certification
  • ICH GCP Refresher (ECCRT, Brussels) in 2013 Certification
  • Clinical Research Training for junior CRAs (ECCRT, Brussels) (Introduction to Clinical research/ Good Clinical Practice/ Essential Documents/ Monitoring activities/ Safety Reporting/ Investigational Product & Supplies/ Quality Assurance/ Understanding in 2012 Certification
  • Communication Skills (ECCRT, Brussels) in 2012 Certification
  • Time Management (ECCRT, Brussels) in 2012 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA)
  • Locations I am interested in:
    Belgium The Netherlands
  • Work From Home:
  • Work Regime:
    BrightOwl freelancer :    24 to 32 hours per week Hours per week
  • International:

Area / Region

Bruges, Belgium


Driving License
  • Yes

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