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Summary

Broad experience in Clinical Trials, mainly phase II-IV and non-interventional/registry studies. Expertise in all stages from start up to close-out: - regulatory submissions - contract negotiations - monitoring

Experiences

Current Experience

  • Clinical Research Associate (CRA)
    Since March 2009

Past Experience

  • Manager, Regional Monitoring
    January 2008 --- February 2009

  • Regional Study Manager
    February 2007 --- December 2007

  • SrCRA
    February 2004 --- January 2007

  • SrCRA
    January 2001 --- January 2004

  • Reg Affairs Manager
    February 1998 --- April 2001

  • Clinical Research Associate (CRA)
    February 1997 --- January 1998

  • Clinical Research Associate (CRA)
    September 1995 --- January 1997

  • Clinical Research Associate (CRA)
    February 1994 --- September 1995

  • Clin Trials Assistant
    September 1990 --- January 1994

Knowledge

LinkedIn Assessment :
Clinical trialsGCPClinical monitoringCTMSCROEDCRegulatory affairsMedical writingICH-GCPPharmacovigilanceClinical DevelopmentDrug DevelopmentInfectious diseasesRegulatory submissionsPharmaceutical IndustryProtocolClinical researchNeurologyMedical affairsSOPClinical Data ManagementTherapeutic AreasHematologyClinical Research AssociatesClinical pharmacologyDrug SafetyGastroenterologyClinical operationsDiabetesClinical Study DesignoncologyEndocrinology

Education

  • BSc in pharm from Uppsala University in 0

Languages

BrightOwl Assessment:
Self Assessment:
Swedish
Native
English
Professional Proficiency

Work Preferences

  • Work From Home:
    Yes, 5 to 0 days per week
  • Work Regime:
    BrightOwl freelancer
  • International:
    Yes

Area / Region

Stockholm County, Sweden

Others

Driving License
  • Yes