I am a biostatistician with over five years of experience in clinical trial design and analysis, currently pursuing a PhD in biostatistics at the University of Sheffield. In my previous role as a Senior biostatistician at Hansen Pharmaceutical, I contributed to multiple trials from early-stage to regulatory submission, working closely with cross-functional teams. I am skilled in statistical programming (SAS, R, Python), adaptive design, Bayesian statistics, and survival analysis.
I have a proven ability to collaborate across teams, ensuring successful trial outcomes and regulatory compliance. My experience includes guiding trial design, preparing statistical analysis plans, and supporting regulatory submissions. I thrive in team environments and am dedicated to contributing to innovative clinical research in Sweden or the United Kingdom.