This book will serve as a quick reference tool for clinical researchers viz. Clinical Research Coordinators (CRCs), Clinical Research Associates (CRAs), Project Managers (PMs), Medical writers, Clinical Trial Investigators etc., and assist them to execute their operational activities in a time bound fashion. The key highlights of this book are: Checklist for Clinical Trial Essential Documents; Checklist for Project Milestone; Checklist for Clinical Trial Protocol Preparation; Checklist for Information Brochure; Checklist for Trial Master File; Checklist for Informed Consent Document; Checklist for Site Initiation, Site Monitoring And Close-Out; Checklist for Ethics Committee Composition; Checklist for Clinical Study Report etc. We hope this book will be of great value to all the clinical trial stakeholders viz. sponsors, investigators, contract research organizations (CROs), ethics committees as well as to those who are aspiring to pursue this field