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Experiences

Past Experience

  • Clinical Research Associate (CRA) Madrid, España

    January 2012 --- April 2015

    medical affairs departament: site selection, prepare site contracts, ethic commite submission, CRO selection,  prepare Pharmacovigilance inspection. 

  • Clinical Research Associate (CRA) Madrid, España

    January 2011 --- November 2011

    i' ve mainly been involved un start up procedures preparing site contracts, file documents, site selection.

    besides, i' ve made several visits  of initiation, monitoring and close up.

Personality

Self Assessment :
AdaptabilityAssertivenessCollaborationIndependenceInterest in knowledgeWillingness to compromise

Knowledge

Self Assessment :
Phase IA rising single dose tolerance study

Skills and Expertise

Self Assessment :
Create SOPs Build and manage the Trial Master File (TMF) Develop clinical trial protocols

Education

  • university degree in life science ( Biology) in Biochemistry and Molecular Biology from University of Oviedo in 2001

Languages

BrightOwl Assessment:
Self Assessment:
English
Elementary Proficiency
Spanish
Native

Work Preferences

  • Notice Period:
    1 week
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Madrid, España

Others

Driving License
  • No

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