Heike Nesbit

Heike Nesbit is an experienced professional in regulatory project management and medical writing, currently serving as the Head of Global Regulatory Project Management at Merck Group since 2012, with prior experience as Director of Regulatory Project and Submission Management and Medical Writing Lead. Previous roles include Senior Medical Writer at Trilogy Writing and Consulting, International Medical Writer at Euro RSCG Life, and Medical Writer at Biologie and Industrie, where responsibilities included authoring healthcare communication materials and Clinical Study Reports. Earlier, Heike Nesbit worked as a Scientist at Cell Genesys, focusing on immunologic testing and assay development for cancer trials. Heike Nesbit holds a PhD in oncology from the University of Pennsylvania and a Doktor Ph.D from the University of Pennsylvania School of Medicine.