Meet our expert Andrea Westerdahl

Andrea Westerdahl joined SDS in 2018 and brought with her substantial experience of a range of studies, from start-up to close-out phase. She honed her skills as a freelance Clinical Research Associate on both large global and local clinical drug development projects where she managed most aspects of the clinical research process.

What is the benefit in employing a CPM advisor?
“With my experience I can guide clients when issues arise during the clinical project.  As I have a passion for designing the correct regulatory compliance study and delivering it on-time, I can lead the study to a successful delivery”.

Andreas work involves protocol design, medical writing, clinical trial submissions and the management of clinical trials, with insight into the small details and the sponsor oversight. Her experience spans pharmaceutical and medical device studies in a variety of therapeutic areas.

“I work in close cooperation with specialists who are performing the clinical trial and I coordinate the process from scientific, regulatory and operational perspectives. I pay close attention to detail.”

Andrea’s educational background is an MSC biochemistry, Linköping University and clinical research from Edinburgh Napier University.

Are you planning a clinical trial? Let Andrea become your guide!