Saurabh Kundgar is a highly experienced Clinical Research professional and trusted industry mentor with years of real-world experience working on global clinical trials across leading pharmaceutical and Contract Research Organizations, including IQVIA, ICON plc, Paraxel, etc.

Unlike purely academic instructors, Saurabh teaches from active industry experience bringing learners inside the real operational world of clinical trials, regulatory compliance, and clinical monitoring.

Throughout his career, he has contributed to the successful delivery of Phase I-IV international clinical studies across diverse therapeutic areas such as Oncology, Vaccines, Diabetes, Cardiology, Gastroenterology, Pulmonology, Psychiatry, and Infectious Diseases.

He has conducted hundreds of site monitoring visits, supported trial start-up to close-out activities, trained junior CRAs, and ensured compliance with global standards including ICH-GCP, FDA regulations, and international clinical trial requirements.

What makes Saurabh’s teaching different?

✅ Industry-first learning approach not textbook theory
✅ Practical workflows used by real CRAs and sponsors
✅ Documentation and TMF skills employers actually expect
✅ Career-focused training designed for job readiness
✅ Simplified explanations of complex regulatory concepts

His courses are built with one mission:

To help learners transition from “knowing clinical research” to confidently working in clinical research.

Thousands of aspiring professionals choose his training to:

- Break into Clinical Research and Pharmacovigilance careers

- Upgrade CRA and clinical operations skills

- Understand real sponsor and CRO expectations

- Build confidence for interviews and industry roles

If you want practical knowledge, industry clarity, and career-ready skills you’re learning from someone who actively works within clinical trials, not just teaches about them.

Learn smarter. Become industry-ready. Build a clinical research career with confidence.