Marco Mazzoletti is a Clinical Scientist and Senior Manager with expertise in oncology. Currently, they manage critical aspects of the study lifecycle at Pfizer, focusing on protocol development, safety data review, and regulatory documentation. Previously, Marco held positions in medical writing and pharmacovigilance at organizations such as Bracco and Pfizer, where they prepared regulatory submissions and safety documents. They hold a PhD in Pharmacology-Oncology from The Open University and have a robust educational background in biotechnology and pharmacology.
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