The CRC's Guide to Coordinating Clinical Research

The CRC's 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 CRC's 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