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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 auditsThe 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
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