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Clinical Research Coordinator Handbook, 5th edition

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Deborrah Norris

Clinical Research Coordinator Handbook, 5th edition Kindle Edition

  • Print length 164 pages
  • Language English
  • Sticky notes On Kindle Scribe
  • Publication date June 17, 2019
  • File size 26529 KB
  • Page Flip Enabled
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  • ASIN ‏ : ‎ B07T7JK2PR
  • Publisher ‏ : ‎ Plexus Publishing, Inc.; 5th edition (June 17, 2019)
  • Publication date ‏ : ‎ June 17, 2019
  • Language ‏ : ‎ English
  • File size ‏ : ‎ 26529 KB
  • Text-to-Speech ‏ : ‎ Enabled
  • Screen Reader ‏ : ‎ Supported
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  • Sticky notes ‏ : ‎ On Kindle Scribe
  • Print length ‏ : ‎ 164 pages
  • #6,769 in Reference eBooks
  • #60,488 in Reference (Books)
  • #134,549 in Nonfiction (Kindle Store)

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clinical research coordinator handbook pdf

By Deborrah Norris

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"This extremely useful title is written for anyone planning to implement clinical trials at an institution. ... the author has carefully detailed the types of forms, study records, and case report forms. ... A powerful appendix and glossary of relevant terms help make this a needed book for any clinical trials office."

— Journal of Hospital Librarianship

In this fully revised and expanded fifth edition of the essential reference for clinical research coordinators, Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The book's five appendices include a directory of CRC resources, updated forms and checklists, state regulatory requirements and contact information, conversion charts and tables, and a glossary.

This book covers these topics and more:

  • Federal Regulations/GCP and ICH Guidelines
  • Clinical Research Coordinator Responsibilities
  • Investigator Responsibilities
  • Obtaining Informed Consent/Assent
  • Creating and Examples of Source Documents
  • Electronic Data Capture (EDC)
  • Preparing for Regulatory Inspections
  • Reporting Study Results

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clinical research coordinator handbook pdf

Clinical Research Coordinator Handbook, 5th edition

$ 43.95

By Deborrah Norris

In this fully revised and expanded fifth edition of the essential reference for clinical research coordinators, Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting.

Description

“This extremely useful title is written for anyone planning to implement clinical trials at an institution. … the author has carefully detailed the types of forms, study records, and case report forms. … A powerful appendix and glossary of relevant terms help make this a needed book for any clinical trials office.”

— Journal of Hospital Librarianship

In this fully revised and expanded fifth edition of the essential reference for clinical research coordinators, Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The book’s five appendices include a directory of CRC resources, updated forms and checklists, state regulatory requirements and contact information, conversion charts and tables, and a glossary.

This book covers these topics and more:

  • Federal Regulations/GCP and ICH Guidelines
  • Clinical Research Coordinator Responsibilities
  • Investigator Responsibilities
  • Obtaining Informed Consent/Assent
  • Creating and Examples of Source Documents
  • Electronic Data Capture (EDC)
  • Preparing for Regulatory Inspections
  • Reporting Study Results

2019 | 168 pages/softbound

Ebook Editions:  Amazon Kindle | B&N Nook | Kobo

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