The guide that has trained thousands of CRAs is updated!
The CRA’s Guide to Monitoring Clinical Research: A definitive resource for building mastery and complying with official regulations and guidelines. Use this guide to advance your career — plus ensure your trials follow critical requirements from FDA, ICH and NIH.
In order to play a leadership role in your clinical research team, you’ll want a firm command of current regulations, as well as good clinical practices and the latest research guidelines.
This 750-page edition of The CRA’s Guide to Monitoring Clinical Research outlines all key CRA job responsibilities, including new digital processes, plus lists all major procedural regulations and guidelines.
Author: Canan Schuman, PharmD/PhD
Canan Schumann is Chief Editor for Axxiem and for Axxiem's blog "BiotechOntheWeb". When not writing for Axxiem, Canan works as a Clinical Research Scientist II at the Research and Development Department at Molecular Testing Labs, developing endpoint assays for the detection of infectious disease and cancer. Canan currently resides in Portland, Oregon, where he received his Honors Bachelor of Science (HBS), Doctor of Pharmacy (PharmD.), and his Doctor of Philosophy (Ph.D.) in Biopharmaceutics at Oregon State University.