I worked in the Pharmacovigilance System Compliance department, where my main job responsibilities was within global compliance tracking and monitoring of submission of adverse event to different stakeholders. Furthermore, I managed a compliance tracking system based on regulatory intelligence, which helped ensure on time reporting and compliance across a global network.

I worked as a GCP-coordinator at the GCP-unit, Copenhagen, where my main job functions were:- Monitoring of investigator-initiated studies in different areas of medicine. - Advisement on how to write a protocol that is to be approved by regulatory authorities.- General guidance on how to fulfill ICH-GCP standards and national legislation during a clinical study- Teaching different personnel about GCP