The CRC's Guide To Coordinating Clinical Research

About this book

The CRCs Guide to Coordinating Clinical Research is a comprehensive training resource for investigative site staff. This invaluable guide offers CRCs the information they need to successfully coordinate a clinical trial from study startup to closeout and beyond. Topics covered include: Developing standard operating procedures (SOPs) Recruiting and retaining study subjects Understanding the informed consent process Working with protocols and case report forms Recognizing adverse events Preparing for audits The CRCs Guide to Coordinating Clinical Research is recommended for: Novice and experienced CRCs Professionals interested in getting involved with clinical research at the investigative site level Investigative site staff