Aniko Molnar

Aniko Molnar is an experienced professional in the clinical trial and regulatory sectors, currently serving as a Country Approval Specialist at PPD since December 2021. Prior to this role, Aniko worked at INC Research for nearly a decade, specializing as a Senior Site Start-Up & Regulatory Specialist, where responsibilities included preparing and submitting clinical trial applications and addressing regulatory queries. Aniko's earlier positions include roles at Amgen Kft and docs as a CTA, focusing on regulatory correspondence and site file preparation. Aniko also served as an Office Head at Zelion, managing client relations and compliance in stem cell services, and worked as a Clinical Trial Administrator at MSD, engaging in data management activities. Aniko holds a Master of Arts degree in philology and classics from Eötvös Loránd University.