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Experience in successfully managing international teams for multinational trials. Focus on oversight, communication, leading cross-functional and remote teams, CRO collaboration, moving ideas from planning into execution phase. Patient recruitment responsible incl online campaigns. Medical device experience. Specialties: Clinical Trials Patient Recruitment Digital Patient Recruitment Site feasibility and site selection Cross-functional Project Management Communication Leading Teams including remote teams CRO collaboration GCP, Medical Device Directive


Current Experience

  • Principal Clinical Study Manager
    Since February 2011
    Current: International Study Manager (program level) for a major Phase III program within Alzheimer's Disease involving 4 global studies, approx +30 countries, 400 sites and 3000 pts . Responsible for Global Patient Recruitment Initiatives (incl digital campaign) as well as planning and execution of task on program level. 2009-2011 International Study Manager for a Phase II Alzheimer's Disease study involving 7 countries, 50 sites and 250 patients.

Past Experience

  • Clinical Operations Manager
    February 2009 --- February 2011
    International Study Manager. Responsible for driving studies from Phase II and forward through planning and conduct including budget responsibility.

  • Clinical Research Manager/ Clinical Program Leader
    May 2003 --- August 2008
    Project management. Clinical study/program planning, design, conduct, follow up and reporting. Outsourcing. Risk management. Regulatory and Marketing support. For Q-Med I worked as a Clinical Study Manager and Clinical Progam Lead of international medical device studies mainly within the esthetic field (wrinkle treatment) Active participation from study in man to achieving CE mark including labelling and initial branding.

  • Clinical Research Associate (CRA)
    September 2000 --- May 2003
    Clinical Research Associate and Clinical Research Manager within asthma, osteoporosis and rheumatology.


LinkedIn Assessment :
GCPClinical trialsMedical Device DirectiveCROClinical operationsCross-functional team leadershipClinical monitoringCTMSClinical DevelopmentICH-GCPRegulatory submissionsClinical researchSOPPharmaceutical IndustryMedical DevicesClinical Study Design


  • Master of Science in Pharmacy from Uppsala universitet in 2000
  • in from Nicolaiskolan in 1994

Area / Region

Helsingborg, Sweden


Driving License
  • No