Clemence Berger

Background

About Clemence Berger

Multidisciplinary professional with academic training in Pharmacy and Law, complemented by extensive international education and regulatory expertise in the pharmaceutical industry. I hold a PharmD (Doctor of Pharmacy) awarded with high distinction in September 2023 and graduated with distinction from the Master’s Degree in International Development and Registration of Medicines and Health Products (DEIM) at Paris-Saclay University, specializing in Regulatory Affairs and Clinical Operations. Currently working as a Senior Regulatory and Start-Up Specialist at IQVIA AG (Basel, Switzerland), where I support clinical trial regulatory submissions and start-up activities in a highly regulated international environment. Within less than a year, I successfully became Country Specialist for Switzerland, leading regulatory strategy and submissions for clinical trials in compliance with Swissmedic, Swissethics and local regulatory requirements. I bring a strong combination of regulatory expertise, analytical thinking, strategical overview, and cross-functional collaboration, with proven ability to adapt quickly, manage complex regulatory frameworks, and contribute to the efficient start-up and execution of clinical studies. I am motivated to continue developing my expertise in global regulatory affairs, clinical development, and pharmaceutical innovation within dynamic and international teams.