FALLS CHURCH, Va.
, Jan. 13, 2020
/PRNewswire-PRWeb/ -- The guide that has trained thousands of CRAs is newly updated.
The CRA's Guide to Monitoring Clinical Research is definitive resource for building mastery and complying with official regulations and guidelines. CRAs use this guide to advance their career and ensure their trials follow critical requirements from FDA, ICH and NIH.
In order to play a leadership role in a clinical research team, CRAs need 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.
As more demands are placed on CRAs, this edition of The CRA's Guide to Monitoring Clinical Research helps them handle them with aplomb.
This guide ensures that CRAs understand new digital developments in clinical research so they can help improve safety reporting, informed consent and patient-reported outcomes.
The CRA's Guide to Monitoring Clinical Research also ensures that CRA's can adopt emerging techniques, such as remote monitoring, wearable devices and tablets and employ them to optimal effect in clinical trials.
Who Will Benefit:
- CRAs or clinical research monitors
- Clinical research managers or other clinical research staff with an interest in study monitoring
- Health professionals interested in pursuing a career as a CRA
- Instructors conducting internal or external training and education programs
The CRA's Guide to Monitoring Clinical Research, 5th Edition **A CenterWatch SOPs Manual** https://www.centerwatch.com/products/category/1060-training-guides/product/348
Easy Ways to Order: Online: https://www.centerwatch.com/products/category/1060-training-guides/product/348 By phone: 617.948.5100 or 866.219.3440
About CenterWatch: Founded in 1994, CenterWatch is a trusted source and global destination for clinical trials information for both professionals and patients. CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, CROs, SMOs, and investigative sites involved in the management and conduct of clinical trials. As a pioneer in publishing clinical trials information, CenterWatch was the first Internet site to publish detailed information about active clinical trials that could be accessed by patients and their advocates.