BrightOwl Loader Loading

Experiences

Current Experience

  • Country Study Manager


    Since May 2007
    have the overall Project Management responsibility for coordinating and managing clinical and epidemiological Phase I-iv trials in Vaccines. accountable for 6-19 simultaneously ongoing trails with the supervisory responsibility for 5-9 cras and ctas (including cros). accountable for quality as well as Budgets. in addition to the above - above country responsibility as the representative for sweden in gsk's european operational network for Clinical trials, european Vaccines & immunotherapeutic Operations network - Planning and running several multi country meetings with cras, ldls and country clin op mangers within europe - Lecturer at external gcp courses for investigators and study nurses in sweden. Have the overall project management responsibility for coordinating and managing clinical and epidemiological phase I-IV trials in vaccines. Accountable for 6-19 simultaneously ongoing trails with the supervisory responsibility for 5-9 CRAs and CTAs (including CROs). Accountable for quality as well as budgets. In addition to the above - Above country responsibility as the representative for Sweden in GSK's European operational network for clinical trials, European Vaccines & Immunotherapeutic Operations Network - Planning and running several multi country meetings with CRAs, LDLs and country clin op mangers within Europe - Lecturer at external GCP courses for investigators and study nurses in Sweden.

Past Experience

  • Clinical Project Manager (CPM)

    January 1997 --- January 2007
    responsible for Phase I - iv trials run in sweden including Clinical trials in asthma/allergy, migraine, Diabetes and social phobia with pet examinations, pediatric and adult Vaccines. responsible for Planning and running Clinical trials from country allocation until site closure, i.e. contacts with central study team, investigators, biobanks, the medical product agency, the Ethics committees and Expert groups, study Applications, monitoring , study completion and reporting.

  • Clinical Research Associate (CRA)

    January 1996 --- January 1997
    responsible for Phase II - iv Clinical trials run in the nordic countries, mainly trials in Infectious diseases. responsible for initiating and monitoring Clinical trials from country allocation until site closure including Applications to the Ethics committee.

  • Clinical Research Associate (CRA)

    January 1996 --- January 1996
    responsible for initiating and monitoring Phase III-iv Clinical trials run in the nordic countries, mainly trials in Gynecology.

  • Clinical Research Associate (Consultant at Upjohn AB)

    January 1995 --- January 1996
    responsible for initiating and monitoring Phase III-iv Clinical trials run in the nordic countries, mainly trials in Gynecology and urology.

  • Laboratory Engineer

    January 1993 --- January 1995
    developed Analytical methods to clarify medical issues. developed a test for helicobacter pylori and an Analysis for detection and to quantification of specific amino acids.

Education

  • Postgraduate education in from Göteborgs universitet in 1994
  • in Organic chemistry (B & C courses, 10 p. + 10 p.) from Chalmers tekniska högskola in 1993
  • Master of Science (M.Sc.) in Chemical and Administrative Science in Science and Business Administration from Karlstads universitet in 1992
  • Naturvetenskaplig linje in Science from Karlbergsskolan, Åmål in 1987
  • High School in from Chaska High School, Minnesota, USA in 1986

Area / Region

Stockholm, Sweden

Others

Driving License
  • No

Similar Candidates

Other Candidates in Sweden

Other Candidates in Stockholm

Other similar Candidates in Stockholm

Other Candidates

Most Recent Searches

Most Famous Searches

You might also like