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I am a graduate in Biomedine with postgraduate training in clinical drug development, an area where I have had my professional career since 2003. Experience of clinical operation and drug development has been gained with the biopharmaceutical industry and with different CROs of sizes from local to world-leading. Across a variety of roles I have developed a broad understanding of the dynamics of project management, site and investigator interactions, and regulatory- and start up processes in clinical trials. I have had the opportunity to work on all phases and in a wide range of therapeutic areas. The various positions have rendered me global knowledge, with focus on Nordics, Europe, Russia and the USA.


Current Experience

  • Director of Clinical Operations
    Since August 2015
    Bringing Glionova's therapeutic candidates through profound clinical studies.

Past Experience

  • Site ID Mgr and Strategic Site Relationship Mgr
    October 2012 --- August 2015
    Accountability for involvement of Investigators in protocols and for feasibility of opportunities in the Nordic countries. Develop and maintain relations with strategic sites.

  • Regulatory and Start Up Manager
    August 2008 --- October 2012
    Global project management of the start up phase of clinical studies.

  • Director of Study Management
    February 2006 --- August 2007
    Project management of phase III studies including CRO selection and management

  • Senior CRA/Project Manager
    August 2003 --- August 2007
    Project management and monitoring of clinical studies primarily in early stage, including all steps from protocol design to report preparation, with coordination of sponsors, functional leads and vendors. Company merged with A+ Science in August 2007

  • Clinical Research Associate (CRA)
    March 2003 --- June 2003
    CRA training, monitoring, feasibility studies at clinical CRO


LinkedIn Assessment :
CROClinical researchPharmaceutical IndustryClinical trialsTherapeutic AreasGCPCTMSoncologyClinical DevelopmentICH-GCPSOPEDCClinical monitoringRegulatory submissionsRegulatory RequirementsProject Management


  • Post-graduate in Clinical Drug Development from Uppsala universitet in 2003
  • M Sc in Biomedicine from in 2001
  • Post-graduate in Microbiology, General from University of Otago in 2000

Area / Region

Uppsala County, Sweden


Driving License
  • Yes