Publisher's Synopsis
This book is an indispensable resource for students and professionals eager to gain a comprehensive understanding of the clinical trial process. The third edition, released in 2025, features 123 chapters, including several new additions and routine updates to existing content.
Clinical research offers a rewarding career path for graduates in medicine, pharmacy, nursing, and other life sciences, with opportunities to work as investigators, scientists, project managers, data managers, monitors, study coordinators, regulatory affairs managers, and more. Transitioning from academia to a career in clinical research can be daunting-something the authors of this book experienced firsthand. While a foundation in drug development is essential, mastering the intricacies of clinical trial planning and management presents its own challenges. This book is designed to bridge that gap. Whether you are a life sciences graduate aspiring to enter the industry or a professional seeking to expand your expertise, this book provides a comprehensive overview of clinical trial operations. It also offers valuable insights for specialists who want to understand the broader landscape of trial planning and management. Since the core principles apply to a wide range of investigational products-including drugs, medical devices, vaccines, and diagnostic agents-this book serves as a valuable resource across the healthcare industry. Structured from the perspective of a trial manager, the book follows the natural lifecycle of a clinical trial-from initial planning to execution and closure-focusing on key activities, roles, and responsibilities. Rather than getting lost in procedural details that vary by organization, it highlights fundamental principles that will help readers navigate the field with confidence.
