Marc Meier-Noorden

Marc Meier-Noorden has extensive experience in regulatory affairs and clinical operations, currently serving as Head of Regulatory Affairs Germany at LEO Pharma since April 2022. Prior to this role, Marc held positions at Leo Pharma GmbH, including Regulatory Affairs & Pharmacovigilance & Quality Assurance Manager from September 2016 to April 2022. Marc's career at Leo Pharmaceuticals spanned over ten years, where responsibilities included Senior Manager of Clinical Trial Management Europe, Head of Clinical Operations Germany, and Clinical Trial Manager/CRA. Earlier experience includes serving as a Clinical Research Associate at Quintiles and as a Scientific Associate at the Paul-Ehrlich-Institut. Marc holds a Diplom-Biologe degree from Goethe University Frankfurt and is trained as a Biologielaborant through the Paul-Ehrlich-Institut.