Introduction To Clinical Reserach: Learn The Basic Building Blocks Of Clinical Trials
Book Details
Author(s)Dan Sfera, John Rahmon
ISBN / ASINB00LAW8QW6
ISBN-13978B00LAW8QW8
Sales Rank369,914
MarketplaceUnited States 🇺🇸
Description
This training program was created to serve as the foundation for anyone looking to get into a career in clinical research, or anyone who is new to the world of clinical trials. I have compressed the most critical elements of clinical research into this quick and easy to read book!
This is the perfect starting point for anyone who is interested in learning the basic building blocks of clinical trials in an easy to understand manner. I cover topics such as Good Clinical Practice, Source Documentation, Case Report Forms, Audits, Working With Monitors, Working With PI’s, Contracts & Budgets, IRB’s, SOP’s and several other fundamental research concepts in great detail while still keeping a concise and well-presented, learning friendly format. I believe that while it may take years to truly become an expert in clinical research, learning the fundamental principles of clinical trials should not require taking dozens of courses or cost thousands of dollars.
This training program is essentially modeled after the same formula that I used to learn clinical trials, and the same formula that I presently use to train all of my employees who work for my various research companies. Through my experiences with monitors, FDA auditors, as well as numerous representatives from CRO’s, Pharmaceutical Sponsors, and IRB’s, my training methods have been approved and even turned into Standard Operating Procedures for several research clinics throughout the years.
I created this program because I saw a need for a beginner’s level training course that introduces some of the most important topics in the world of clinical research.
This is the perfect starting point for anyone who is interested in learning the basic building blocks of clinical trials in an easy to understand manner. I cover topics such as Good Clinical Practice, Source Documentation, Case Report Forms, Audits, Working With Monitors, Working With PI’s, Contracts & Budgets, IRB’s, SOP’s and several other fundamental research concepts in great detail while still keeping a concise and well-presented, learning friendly format. I believe that while it may take years to truly become an expert in clinical research, learning the fundamental principles of clinical trials should not require taking dozens of courses or cost thousands of dollars.
This training program is essentially modeled after the same formula that I used to learn clinical trials, and the same formula that I presently use to train all of my employees who work for my various research companies. Through my experiences with monitors, FDA auditors, as well as numerous representatives from CRO’s, Pharmaceutical Sponsors, and IRB’s, my training methods have been approved and even turned into Standard Operating Procedures for several research clinics throughout the years.
I created this program because I saw a need for a beginner’s level training course that introduces some of the most important topics in the world of clinical research.
