Publisher's Synopsis
Clinical Research Pearls is a compact, wisdom-rich guide that distills the complexities of clinical trial conduct into 255 practical tips-or "pearls"-tailored for investigators, coordinators, monitors, and aspiring research professionals. Designed to serve both as a day-to-day reference and a strategic resource for certification prep (e.g., ACRP, SoCRA, GCP), this book covers the entire clinical research lifecycle.
Organized across 16 thematic chapters, each pearl provides concise, experience-based guidance on essential topics, including:
Study start-up and protocol development
Ethics and informed consent
Roles and responsibilities of the research team
Site and regulatory file management
Subject recruitment and retention strategies
Safety reporting, investigational product handling, and audits
Leadership, mentorship, and building a quality-focused research culture
Managing protocol deviations and regulatory noncompliance
To complement the pearls, the book includes 100 flashcards-ideal for exam revision, quick knowledge checks, or team training sessions. These cards reinforce high-yield facts, common acronyms, and essential GCP concepts.
This book is perfect for:
Principal Investigators (PIs) seeking better oversight strategies
Clinical Research Coordinators (CRCs) managing daily trial operations
Monitors/CRAs ensuring quality and compliance at trial sites
Research students and trainees preparing for entry-level roles or exams
Whether you're a newcomer or a seasoned research professional, Clinical Research Pearls delivers bite-sized, actionable knowledge that promotes excellence, compliance, and ethical trial conduct across every phase of research.
