Role and Responsibilities of a Clinical Research Associate in Clinical Trials

Role and Responsibilities of a Clinical Research Associate in Clinical Trials offers an in-depth exploration of the CRA’s pivotal role in ensuring ethical scientific and regulatory compliance throughout a clinical trial. Written by experienced professionals the book covers every phase of study execution — from site qualification and initiation to monitoring audit preparedness and study closure — aligned with NDCT 2019 ICH-GCP E6(R3) and ICMR 2017 guidelines. It blends practical insights with ethical reflections providing readers with both operational knowledge and professional perspective. Designed for aspiring and practicing CRAs site coordinators and clinical research professionals this book serves as a comprehensive reference and a guide for excellence in clinical research practice. A must-read for those who value accuracy ethics and accountability in the advancement of medical science.