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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


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; 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 - 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


LinkedIn Assessment :
Clinical monitoringClinical trialsCommunicationDiabetesGCPoncology


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


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Area / Region



Driving License
  • Yes