Prerna Arora

I am a clinical research professional with over seven years managing device-based trials, wearable health-tech studies, early-phase drug trials (Phase 1b), and AI-driven clinical research. I specialize in protocol development, regulatory compliance, patient recruitment, and cross-functional coordination.

At Stanford School of Medicine I managed multi-phase medical device and wearable technology clinical trials end-to-end, reduced study startup delays by 30%, and increased enrollment by 20% while maintaining 100% protocol compliance. I maintained flawless eTMF accuracy and supported 15+ SIVs, monitoring visits, and close-outs, passing audits with zero major findings.

I routinely author regulatory documents and SOPs and have trained junior staff to improve data quality and protocol adherence. I analyze study data using tools such as REDCap, Excel, and Clintrak to surface trends that inform protocol amendments and operational strategies.

I hold an M.Tech in Industrial Biotechnology and certifications in Clinical Research Conduct and Management, IRB BioMed/GCP Research, and Google Data Analytics. I am a co-author on 16+ peer-reviewed publications across clinical research, medical devices, AI in healthcare, and proteomics.