The CRC's Guide To Coordinating Clinical Research
<i>The CRC's Guide to Coordinating Clinical Research</i> 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. <BR><BR>Topics covered include:<BR>*Developing standard operating procedures (SOPs) <BR>*Recruiting and retaining study subjects <BR>*Understanding the informed consent process <BR>*Working with protocols and case report forms <BR>*Recognizing adverse events <BR>*Preparing for audits <BR><BR><i>The CRC's Guide to Coordinating Clinical Research</i> is recommended for: <BR>*Novice and experienced CRCs <BR>*Professionals interested in getting involved with clinical research at the investigative site level <BR>*Investigative site staff