Laura Rodriguez

Laura Rodriguez is a seasoned professional in clinical research with extensive experience in regulatory affairs and startup processes. Currently serving as a Principal Country Approval Specialist at PPD since March 2022, Laura has previously held significant roles at Labcorp Drug Development and IQVIA, where responsibilities included regulatory strategy planning and project activation for clinical studies. Laura's career began at The Janssen Pharmaceutical Companies of Johnson & Johnson, working in various regulatory and research development capacities. Educationally, Laura earned a degree in Pharmacy from the Universidad de Buenos Aires, which supplements a robust background in navigating regulatory frameworks across multiple South American countries.