Florence Beck
About Florence Beck
Florence Beck is the Vice President of Clinical & Regulatory Affairs, with nearly two decades of experience in supporting regulatory submissions and market strategies through evidence generation.
Florence Beck - VP of Clinical & Regulatory Affairs
Florence Beck serves as the VP of Clinical & Regulatory Affairs. With nearly two decades of experience, she specializes in generating evidence to support regulatory submissions on both national and international levels. Her work includes health economics initiatives and strategies for market adoption. Florence's extensive background in clinical and regulatory affairs positions her as a key player in her field.
Florence Beck's Education and Expertise
Florence Beck holds an undergraduate degree in Microbiology from the University of Florida. She further enhanced her expertise by obtaining a master's degree in Regulatory Affairs from Northeastern University. This educational foundation supports her almost 20-year career dedicated to clinical and regulatory affairs.
Florence Beck's Background in Research Projects
Florence Beck has extensive experience in building and managing a wide range of research projects. Her portfolio includes investigator-initiated studies, large post-market registries, and randomized controlled multicenter trials. Her management proficiency in these areas has significantly contributed to the success of the projects she has overseen.
Florence Beck in Regulatory Submissions and Health Economics
Florence Beck's career is marked by nearly two decades of expertise in generating crucial evidence to support regulatory submissions. Her role extends beyond clinical aspects, encompassing health economics initiatives that lay the groundwork for effective market adoption strategies. Her contributions are integral to both national and international regulatory landscapes.