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Summary

high quality-orientated Clinical Research Professional with solid credentials in: - medical/scientific review of protocols - scientific support to internal departments - liaising with therapeutic experts in the field - Clinical Trial feasibility assessments early and late phase trials - Patient Recruitment early phase - Line Management - advanced gcp knowledge - full cycle Clinical Trial monitoring - trial management Software Trainer - Sourcing study related material and vendor liaising - Clinical Research Physician activities - significant australasian exposure in Clinical Trial environment exposed Therapeutic Areas: Respiratory, Infectious diseases, gynaecology, CNS, Psychiatry Diabetes, Cardiology, oncology

Experiences

Current Experience

  • Sr. Associate Medical Director


    Since April 2016

Past Experience

  • Head Feasibility and SMO Europe - Clinical Research

    April 2012 --- April 2016
    early and late phase patient study feasibilities - medical/scientific review of protocols - liaising with kol, therapeutic experts, patient organisations - medical/scientific support to internal departments - site identification - site prospect visits - establishing collaborations with Hospitals - Patient Recruitment at sgs cpu - client meetings - bid defense meetings - set-up feasibility department - Line Management of the feasibility team - Line Management of the site management organisation team

  • Feasibility Support and KOL Manager

    March 2012 --- April 2012
    - assessing feasibility of late phase studies within europe - identifying sites and investigators across a diversity of Therapeutic Areas - supporting the smo and bd team

  • Clinical Research Associate (CRA)

    January 2007 --- May 2011
    full cycle monitoring, including site feasibility and Ethics /ra submissions; Report Writing; site management; Investigator meetings organisation; trial management Software Trainer; vendor Sourcing, liaising and negotiations; science)" rel="nofollow">Protocol and icf writing; Pharmacovigilance assistance; rfp coordination; eCRF: inform and pds

  • Clinical Trials Coordinator

    July 2005 --- December 2006

  • Clinical Research Physician

    October 2004 --- December 2004
    early phase studies - science)" rel="nofollow">Protocol and ib review; consenting, screening and follow-up of participants; ae reviewing and reporting

  • Customer Relations Officer

    October 2002 --- December 2003
    Medical Device company - set-up and managment of customer relation department; providing advice to end-consumers/patients; managing product-related issues and complaints

Knowledge

LinkedIn Assessment :
Clinical monitoringClinical trialsCommunicationDiabetesGCPoncology

Education

  • Graduate Certificate in Drug Development from University of New South Wales in 2008
  • Master in Medicines from Katholieke Universiteit Leuven in 2001

Languages

BrightOwl Assessment:
Self Assessment:
English
Full Proficiency
Dutch
Native

Area / Region

Belgium

Others

Driving License
  • Yes

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