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22 years experience in Clinical Research as Study-Leader and Senior Clinical Research Associate, particularly in Oncology. 18 years as Aid'ARC sarl Manageress: a team of 3 experienced Study-Leaders/ Senior CRAs. 10 years as OPTIMARC Network President. Experience as CRA : Investigators recruitment and screening, Pre-Study Visits, Initiation Visits, Monitoring Visits and Close-out Visits, Site Coordination. Experience as Study Leader : Clinical trial management (administrative and regulatory initiation of the study, creation of the study monitoring guideline, management of the sites financial contracts , SAEs follow-up), CRAs training and management. Experience as Study-Coordinator: CRF completion, patient visits organization, ... Therapeutics areas of experience : Cardiovascular, Cardiology, Dermatology, Endocrinology, Gerontology, Gynaecology, Haematology, Infectiology, Neurology, Oncology, Ophthalmology, Pneumology, Psychiatry, Renal System, Rheumatology Expert in Oncology and Respiratory.


Current Experience

  • Senior CRA/Study Leader
    Since October 1998

Past Experience

  • President
    January 2005 --- January 2015
    OPTIMARC is a French Network of Free-lance Senior Clinical Research Associates (30 SCRAs)

  • Lead CRA in Cardiovascular
    June 1997 --- September 1998

  • Oncology Senior CRA
    June 1994 --- May 1997


LinkedIn Assessment :
oncologyRecherche cliniqueEssais cliniquesBonnes pratiques cliniques


  • Training of “French and European Regulatory of EC submission regarding drugs and medical devices” in from SUNNIKAN Consultants in 2011
  • Study-Leader Training in from SANOFI-AVENTIS in 1997
  • Oncology Training in from Institut Gustave Roussy, Villejuif in 1995
  • Clinical research Associate in from ARCAM, Paris in 1994
  • Jan 2016: The new European rule in Clinical studies (Guideline 2001/20/CE) in from IFIS in 0


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Area / Region

Palaja, France


Driving License
  • Yes