I have a background from the pharma industry and AstraZeneca where I worked as a SAS-programmer with clinical trials. I was also responsible for the implementation of the industry data standard (CDISC) for clinical trial data in preparations for regulatory submissions.
I'm interested in developing common methods and processes through improvement projects. At the Center for Pharmacoepidemiology (CPE), I have together with Professor Morten Andersen, University of Copenhagen, developed a Nordic Common Data Model (CDM) that will lead to more efficient data management using health register data from e.g. Swedish National Board of Health and Welfare and Statistics Sweden. The hope is that CDM can support Nordic collaborations and to make pharmacoepidemiological research more transparent. At CPE I have led the work of developing a quality management system to meet demands from regualtory authorities when conducting commissioned projects as well as academic studies in the pharmacoepidemiological field. I'm also acting as a project manager for a number of Post Authorisation Safety Studies (PASS).
- B.Sc. in Behavioural Research with advanced studies in Sociology, Stockholm University
- SAS Certified Developer
Karolinska vägen 171 76 Solna