Monitoring Clinical Trials: A CRAs job description

Monitoring Clinical Trials: A CRAs job description

<br /><b>***Amazon Prime and Kindle Unlimited members; Yes, you can download this book for FREE on your Kindle device***</b><br /><br />What is a clinical research associate?”... is a question I hear time and time again. In a nutshell, it is an exciting job in the healthcare industry and this book will break it down in easy to understand steps. The job of a clinical research associate can sometimes look complex. It does indeed have a lot of moving parts, but, it is straight forward and can be easily picked up. However, because it requires a detailed oriented and hard working individual to monitor trials, JP Holdasham decided to share his experiences with other folks interested in learning more about being a clinical research associate(CRA) or monitor. <br /><br />Like every other career, you learn the core components; become an expert in them and as your experience increases by... “doing the job” you become an expert. BY working with for Contract research organizations (CRO) as a CRA you participate in new drug trials that could involve Phases I – Phase IV. You work with the principal investigator (PI), the clinical research coordinator (CRC) under GCP and ICH guidelines to ensure the well being of the trial subjects and integrity of the trial.<br /><br />Monitoring Clinical Trials will introduce you to the core duties of a clinical research monitor, how they prepare for any of their monitoring visits