Puloma Pandey

Clinical Operations professional with 8+ years of experience across sponsor, CRO, and academic research environments, specializing in end-to-end clinical trial management, site operations, and TMF oversight. Proven expertise in trial startup, regulatory submissions, site coordination, and inspection readiness across Phase II & III studies. Strong track record in driving GCP compliance, managing cross-functional stakeholders, improving trial efficiency, and leading teams to deliver high-quality, audit-ready clinical trials.