The CRC's Guide to Coordinating Clinical Research, Fourth Edition

Sandra Sather

ISBN 10: 1604301007 / ISBN 13: 9781604301007

Published by CenterWatch, 2019

About this Item

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Bibliographic Details

• Title: The CRC's Guide to Coordinating Clinical Research, Fourth Edition
• Publisher: CenterWatch
• Publication Date: 2019
• Language: English
• ISBN 10: 1604301007
• ISBN 13: 9781604301007
• Binding: Perfect Paperback
• Edition: 4th Edition
• Condition: Good

About this title

Synopsis

The CRC's Guide to Coordinating Clinical Research, 4th edition, is the most comprehensive, easy-to-read training guide for novice and experienced clinical research coordinators. The newly-released fourth edition includes industry facts, insights on the role and responsibilities, personal experiences to learn from, checklists to help you be successful and efficient as a CRC, key takeaways, case studies and much more on this important role in the clinical research industry.

The CRC Guide is the ideal go-to resource for professionals interested in pursuing a clinical research coordinator position as well as an easy-to-reference training guide for experienced CRCs, on-site professional development courses and professors teaching courses in this field.

About the Author

Sandra Sather has over 30 years of clinical experience, a Bachelor of Science degree in Nursing and a Master of Science degree in Education with a Specialization in Training and Performance Improvement. She has served many roles in clinical research including site study coordinator and manager, sponsor and CRO monitor, quality assurance auditor, risk manager, trainer and performance management consultant. SAM has held clinical research certifications for over 15 years by the Association for Clinical Research Professionals (ACRP). She is a current member of the ACRP Academy Board of Trustees and the Regulatory Affairs Committee (RAC).

Sandra is a frequent subject-matter expert for GCP regulation and a speaker at industry conferences. She is a strong advocate for research sites and supports the sites that establish quality systems to support the investigator oversight of clinical trials to ensure human subject protection, data integrity and site performance excellence. SAM has authored dozens of competency-based curriculums for study coordinators and site monitors.