Martin Simicek is a seasoned professional in regulatory affairs, currently serving as the Global Domain Lead for Veeva Submissions Publishing. With extensive experience at Veeva Systems from 2020 to 2022 in various consultant roles, Martin specialized in RIM solution implementations. Prior to this, Martin worked for Angelini as a Regulatory Affairs Specialist, overseeing product authorization and electronic submissions. Martin also held positions at ASPHALION and participated in multiple internships and trainee roles in the pharmaceutical sector, demonstrating a broad expertise in regulatory activities and compliance. They hold a Master of Pharmacy degree from the University of Veterinary and Pharmaceutical Sciences Brno, completed in 2016.
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