Description
Book Synopsis: 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
Details
Are you a clinical research coordinator (CRC) looking for a comprehensive training resource? Look no further than The CRC's Guide to Coordinating Clinical Research. This invaluable guide has everything you need to successfully coordinate a clinical trial from study startup to closeout and beyond.
With topics ranging from developing standard operating procedures (SOPs) to understanding the informed consent process, this guide covers it all. You'll learn how to recruit and retain study subjects, work with protocols and case report forms, and recognize adverse events. With this guide, you'll be well-prepared for any audits that come your way.
Who is this guide recommended for? Novice and experienced CRCs, as well as professionals interested in getting involved with clinical research at the investigative site level. Whether you're just starting out or looking to enhance your skills, this guide is for you.
Don't miss out on this incredible resource. Get The CRC's Guide to Coordinating Clinical Research now and take your coordination skills to the next level.
Click here to start your journey towards becoming a proficient CRC!
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