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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 0000


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Area / Region

Palaja, France


Driving License
  • Yes

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