Sheetal Haria

Sheetal Haria has extensive experience in regulatory affairs and clinical trial management, having worked in various roles since 2002. At Quest Diagnostics, Sheetal served as a Medical Laboratory Assistant and investigator site coordinator before advancing to regulatory affairs at ORION Clinical Services, where responsibilities included drafting clinical trial applications and regulatory documentation. Further experience was gained at PPD as a Regulatory Affairs Executive, focusing on multinational clinical trials and compliance with regulatory guidelines. Subsequent positions included Senior Global Regulatory Affairs Specialist at Worldwide Clinical Trials and Director, Study Start-Up at TFS - Clinical Contract Research Organization. Currently, Sheetal is a Regulatory Affairs Consultant at Novotech, contributing expertise to regulatory submissions and project management within the clinical trial sector.