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PROFILE • Currently working with Oncology and Neonatology as Sr CRA • Extensive Clinical Project experience across different therapeutic areas and different phases • Excellent time management skills • Aspirational and responsibility taking • Ability to learn new tasks and assignments quickly • Positive and open to mentoring junior colleagues Clinical project experience - Global Phase IV study - Multiple Sclerosis - Monitoring, Norway - Global Phase III study - Oncology - Monitoring, Norway, Denmark - Global Phase II study - Neonatology - Study start up, monitoring, Lead - Global Phase III study - Multiple Sclerosis - Project management,monitoring, co-monitoring - Global Phase IV study Multiple Sclerosis – Site management, monitoring 17 sites - Global Phase IV study Ulcerative Colitis – Site management, monitoring 5 sites - Global Phase IV study Cardiology – Site management, monitoring 14 sites - National Phase II study, Neuropathic pain, Site management, monitoring, 1 site - Global Phase III study Hyperlipidemia – Application to CA, Ethics and biobank submission Therapeutic Area of Expertise Oncology, Pain, Cardiology, Hyperlipidemia, Multiple Sclerosis, Gastroenterology, Ulcerative Colitis, Allergy, CNS, Parkinson, PMDD, Fertility, Neonatology


Current Experience

  • Clinical Research Associate (CRA)
    Since September 2015
    Looking for new opportunities within CRM, CRA, BD. Looking forward hearing from you

Past Experience

  • Clinical Research Associate (CRA)
    May 2013 --- September 2015
    Monitor, CRA, Project Management

  • Clinical Research Associate (CRA)
    January 2011 --- April 2013
    During the time I worked at IRW, I also worked from Stockholm, Sweden

  • Regulatory Affairs Coordinator
    October 2010 --- January 2011
    Product Quality complaints

  • Pharmacist
    September 2010 --- October 2010
    Travelling Pharmacist

  • Pharmacist
    August 2010 --- October 2010

  • Student
    January 2009 --- June 2009
    Bachelor thesis -Branding


LinkedIn Assessment :
Pharmaceutical IndustryGCPICH-GCPClinical DevelopmentRegulatory submissionsCROClinical researchLifesciencesClinical monitoringDrug DevelopmentSOPCardiologyProtocolClinical Study DesignPharmacokineticsClinical trialsoncologyRegulatory affairsDrug DiscoveryPharmacovigilanceCTMSpharmacologySOPLife Sciences


  • Bachelor degree in Business Administration from Uppsala universitet in 2010
  • Graduate Course in Clinical Drug Development from Uppsala University in 2010
  • M.Sc in Pharmacy from Uppsala University in 2010
  • Bachelor of Business Administration in Business Administration from University of Sydney in 2008

Training and Certification

  • Graduate Course, Clinical Drug Development Certification

Area / Region



Driving License
  • No