Rosey Oboh

Rosey Oboh is a seasoned clinical research professional with extensive experience in clinical trial management. Currently serving as a Senior Clinical Research Associate at Parexel since August 2020, Rosey Oboh is responsible for monitoring clinical research studies and ensuring timely documentation of Adverse Events and Serious Adverse Events while maintaining compliance with sponsor requirements and Good Clinical Practice (GCP). Previously, Rosey Oboh held multiple roles at IQVIA Biotech from May 2014 to July 2020, culminating in the position of Clinical Research Associate II, focusing on regulatory compliance and site monitoring. Earlier experience includes work as a Clinical Research Coordinator at Duke University, where study-related materials were developed and regulatory packages reviewed.