Rikke Lillesø

Rikke Lillesø has diverse work experience in regulatory affairs and project management within the pharmaceutical industry. Rikke currently holds the position of Vice President at Y-mAbs Therapeutics, Inc. since January 2019. Prior to this, they served as the Director of Regulatory Affairs at the same company from November 2017 to December 2018.

Before joining Y-mAbs Therapeutics, Inc., Rikke worked at Zealand Pharma A/S as a Senior Regulatory Project Manager from February 2016 to October 2017. Rikke also had a long tenure at Novo Nordisk, where they held several positions including Senior Regulatory Project Manager, Regulatory Project Manager, Nonclinical Project Manager, and Regulatory Professional between 2006 and 2016.

Rikke's early career includes roles as a Regulatory Professional at LEO Pharma A/S from January 2005 to July 2006, and as a Project Manager and Regulatory associate at Medico-Chemical Lab ApS from August 2002 to December 2004.

Throughout their career, Rikke has showcased their expertise in global regulatory strategies, clinical trial applications, health authority interactions, drug development plans, cross-functional and cross-project cooperation, and regulatory consulting within pharmaceuticals and related industries.

Rikke Lillesø obtained a Diploma in Managing Medical Product Innovation from Copenhagen Business School in 2014-2015. Prior to that, Rikke earned another Diploma in Regulatory Affairs from Medicademy in an unspecified period. Rikke also possesses a MSc degree in Food Science and Technology from DTU - Technical University of Denmark, which was completed between 1997 and 2003.