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Experiences

Current Experience

  • Clinical Research Specialist - Sr CRA - Project Management
    Since March 2011
    Freelance clinical research work in following therapeutic domains : - Hematology (pediatric and adult pathology) - Endocrinology (pediatrics) - HIV/HCV - Urology - Oncology (Breast, Prostate, NSCLC, Hodgkin, ...) - rhumatology - neurology (MS) - Cardiovascular diseases - Intensive Care (CPR, ARDS) - Medical devices (cardiac valves, cardiac and vascular stents) As Clinical Research Professional, I have a broad experience in EC/CA submission, monitoring work (all the way from start-up to close-out), project management, contract/budget negotiation, ...

Past Experience

  • Senior Clinical Research Associate (CRA)
    July 2009 --- February 2011
    @ Wyeth pharmaceuticals Benelux and Novartis GenMed

  • Site Management Coordinator
    August 2008 --- June 2009

  • Junior CRA
    July 2006 --- June 2008
    @ GlaxoSmithKline Pharmaceuticals Genval and @ Wyeth Pharmaceuticals Benelux

  • Nurse
    August 1999 --- June 2006
    intensive care nursing

Knowledge

LinkedIn Assessment :
Clinical monitoringICH-GCPGCPCTMSClinical researchClinical Research AssociatesClinical trialsHematologyoncologyNeurologyCROClinical DevelopmentEDCPharmaceutical Industry

Skills and Expertise

Self Assessment :
Build and manage the Trial Master File (TMF) Interact with nurses Interact with physicians Monitor a clinical study Report dataAct as the main line of communication between the sponsor and the investigator

Education

  • RN in from in 1999

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Full Proficiency
French
Full Proficiency
German
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA) Project Manager
  • Work From Home:
    No
  • Work Regime:
    BrightOwl freelancer :    40 Hours per week
  • International:
    Yes

Area / Region

Genk

Others

Driving License
  • Yes