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Summary

i am responsible for the local Project Management of different oncology and Nephrology projects in belgium, luxemburg, israel, turkey and south africa for amgen, a large Biotechnology company.

Experiences

Current Experience

  • Regional Medical Liaison


    Since January 2015

    as rml, my primary responsibility is to interact with Healthcare decision makers in belgium to communicate and advance the scientific platform as aligned with amgen’s corporate goals and objectives.

    As RML, my primary responsibility is to interact with healthcare decision makers in Belgium to communicate and advance the scientific platform as aligned with Amgen’s corporate goals and objectives.

Past Experience

  • Clinical Operations Manager

    February 2011 --- December 2014

    main functions responsible for local science)" rel="nofollow">Protocol and site feasibility assessment local Planning, execution, management and reporting on amgen sponsored studies therapeutic domain oncology, Nephrology, Inflammation geography belgium, luxemburg, israel, south africa & turkey

  • contractor

    January 2008 --- January 2013

  • senior associate clinical operations manager

    June 2009 --- January 2011
    valesta nv, mechelen; outsourced to amgen, brussels main functions support Clinical operations managers with overseeing operational activities related to Planning, executing, and reporting of Phase 3 and 4 amgen sponsored Clinical trials. support amgen specific operational activities related to the Planning, review/approval and implementation support of Investigator sponsored studies. therapeutic domain oncology, Nephrology, Cardiology geography belgium, luxemburg, israel, south africa

  • associate Clinical Project Manager

    January 2008 --- June 2009
    valesta nv, mechelen; outsourced to ucb pharma, braine l’alleud main functions providing operational support to cpm, co-monitoring visits, coordination and follow-up on crf retrieval and query resolution, CRA Training, review and follow up of monitoring reports therapeutic domain epilepsy geography eastern and western europe & asia

  • Clinical Research Associate (CRA)

    January 2005 --- January 2008
    main functions monitoring Clinical trials in belgium which included submission to Ethics committee, initiations, monitoring, close-out and archiving extra functions participation to local workgroups on standard operating procedures, Training and Coaching of junior cras, from february 2007 to january 2008, i was appointed as local Expert for the implementation of electronic crfs in sanofi-aventis belgium therapeutic domains oncology, Cardiology, Internal medicine, thrombosis and osteogenesis imperfecta

Skills and Expertise

BrightOwl Assessment :
Answer, transfer and handle incoming calls as needed.

Education

  • in from Katholieke Universiteit Leuven in 2004
  • in from Katholieke Universiteit Leuven in 2003

Languages

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

Work Preferences

  • Work From Home:
    No
  • Work Regime:
    Permanent position
    BrightOwl freelancer :    40 Hours per week
    BrightOwl employee
  • International:
    No

Area / Region

Linden - belgium

Others

Driving License
  • Yes

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