My role is responsible for planning, coordinating and executing clinical trials and other tasks within clinical development. In addition my contribution is to give input to protocols and statistical analyses, analyzing and interpreting trial results and handle day-to-day statistical issues during the course of the trial. My support activities include input to manuscripts, risk management plans and other safety reports, presentation and discussion of results and coordination of research groups

ORCID ID

http://orcid.org/0000-0001-8086-6362

Reviewer Keywords