Sandra Nantumbwe

Sandra is a clinical research professional with over five years of experience working across multidisciplinary research and clinical trial environments. My experience includes GCP compliance, protocol adherence, clinical trial monitoring, regulatory submissions, audit readiness, and quality management systems. 

As Quality and Regulatory Affairs Manager within the CRSU, Sandra supports researchers in navigating regulatory and ethical requirements and maintaining high standards of research quality. Her role also provides guidance on documentation, regulatory compliance, and quality processes to help researchers conduct their work safely, consistently, and in accordance with approved protocols, applicable regulations, and ethical standards. Through this support, Sandra aims to help researchers navigate the requirements of clinical research with confidence while maintaining the highest standards of quality and participant safety.