I'm leading pre-clinical and clinical trial operations at Cepheid in Sweden, coordinating planning, budgets, resources, eCRF activation, protocols, site activities, and cross-functional delivery.
Previously at Syneos Health, I led global multi- and single-sponsor studies across EMEA and North America, owning timelines, budgets, forecasts, risk management, inspection readiness, and sponsor governance. I also mentored Project Managers, CRAs, and project support staff while supporting bid defenses and proposal development.
My work at Eli Lilly, PRA Health Sciences/ICON, and Syneos Health has covered study start-up, maintenance, close-out, site management, clinical contracts, regulatory submissions, monitoring oversight, and Trial Master File management. I've supported studies across oncology, infectious diseases, neurology, hematology, cardiology, nephrology, rare diseases, and anesthesiology.
I bring more than 10 years of experience working across EMEA, APAC, North America, and LATAM, with a focus on ICH-GCP compliance, risk-based monitoring, financial accountability, and practical collaboration across clinical, regulatory, legal, finance, and commercial teams.
