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Current Experience

  • Regulatory Affairs Manager Brussels, Belgium
    Since December 2014

  • Regulatory Affairs Specialist
    Since June 2012
    - Direct the preparation and submission of regulatory agency applications, reports, or correspondence. - Review all regulatory agency submission materials to ensure timeliness, accuracy, comprehensiveness, or compliance with regulatory standards. - Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products. - Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced. - Communicate regulatory information to multiple departments and ensure that information is interpreted correctly.

Past Experience

  • Regulatory Affairs Assistant
    June 2011 --- June 2012

  • General Secretary - CDD
    March 2009 --- September 2009

  • commercial and administrative employee
    April 2006 --- December 2008


Self Assessment :
CollaborationProblem solving


LinkedIn Assessment :
Regulatory affairsClinical researchRegulationsPharmaceutical IndustrySOPClinical trialsoncologyGCPClinical DevelopmentBiotechnology


  • certificate in commerce international from CEFORA in 2009
  • Candidacy - translation English-Italian in from Haute Ecole Francesco Ferrer in 2001
  • in French Language and Literature from IFCAD - French Courses in 1997
  • Bachelor's degree in Veterinary medecine from Baghdad University in 1995
  • Baccalaureate in General Studies from Bagdad High School in 1990

Work Preferences

  • Notice Period:
    4 weeks
  • Work From Home:
    Yes, 1 to 2 days per week
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:

Area / Region



Driving License
  • No