Description

Book Synopsis

A Practical Guide to Managing Clinical Trials is a basic, comprehensive guide to conducting clinical trials. Designed for individuals working in research site operations, this user-friendly reference guides the reader through each step of the clinical trial process from site selection, to site set-up, subject recruitment, study visits, and to study close-out. Topics include staff roles/responsibilities/training, budget and contract review and management, subject study visits, data and document management, event reporting, research ethics, audits and inspections, consent processes, IRB, FDA regulations, and good clinical practices. Each chapter concludes with a review of key points and knowledge application.

Unique to this book is A View from India, a chapter-by-chapter comparison of clinical trial practices in India versus the U.S. Throughout the book and in Chapter 10, readers will glimpse some of the challenges and opportunities in the emerging and

Trade Review

'"A Practical Guide to Managing Clinical Trials" provides a good introduction to the basics of clinical research for investigators, study coordinators, and other site personnel. The clear writing makes the book a quick read.'
Norman M. Goldfarb for Journal of Clinical Research Best Practices, Vol. 13, No. 12, December 2017.


'"A Practical Guide to Managing Clinical Trials" provides a good introduction to the basics of clinical research for investigators, study coordinators, and other site personnel. The clear writing makes the book a quick read.'
Norman M. Goldfarb for Journal of Clinical Research Best Practices, Vol. 13, No. 12, December 2017.



Table of Contents

Chapter 1: Rules, Roles and Responsibilities

Chapter 2: Products, Protocols, and Pre-trial Preparation

Chapter 3: Sponsor, Site and Study Start-up

Chapter 4: Enticement, Enrollment, and Engagement: The Informed Consent Process

Chapter 5: From Enrollment to Final Visit

Chapter 6: Collaborating for Compliance and Quality Data – Monitoring and Audits

Chapter 7: Building Budgets

Chapter 8: Contracts, Clauses and Closing the Deal

Chapter 9: US Clinical Trials – Additional Topics

Chapter 10: Clinical Research and India

A Practical Guide to Managing Clinical Trials

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    Order before 4pm today for delivery by Mon 29 Jun 2026.

    A Hardback by JoAnn Pfeiffer, Cris Wells

    1 in stock

      Trusted by thousands of customers. See 2,385+ Customer Reviews

      View other formats and editions of A Practical Guide to Managing Clinical Trials by JoAnn Pfeiffer

      Publisher: Taylor & Francis Ltd
      Publication Date: 17/05/2017
      ISBN13: 9781138196506, 978-1138196506
      ISBN10: 1138196509

      Description

      Book Synopsis

      A Practical Guide to Managing Clinical Trials is a basic, comprehensive guide to conducting clinical trials. Designed for individuals working in research site operations, this user-friendly reference guides the reader through each step of the clinical trial process from site selection, to site set-up, subject recruitment, study visits, and to study close-out. Topics include staff roles/responsibilities/training, budget and contract review and management, subject study visits, data and document management, event reporting, research ethics, audits and inspections, consent processes, IRB, FDA regulations, and good clinical practices. Each chapter concludes with a review of key points and knowledge application.

      Unique to this book is A View from India, a chapter-by-chapter comparison of clinical trial practices in India versus the U.S. Throughout the book and in Chapter 10, readers will glimpse some of the challenges and opportunities in the emerging and

      Trade Review

      '"A Practical Guide to Managing Clinical Trials" provides a good introduction to the basics of clinical research for investigators, study coordinators, and other site personnel. The clear writing makes the book a quick read.'
      Norman M. Goldfarb for Journal of Clinical Research Best Practices, Vol. 13, No. 12, December 2017.


      '"A Practical Guide to Managing Clinical Trials" provides a good introduction to the basics of clinical research for investigators, study coordinators, and other site personnel. The clear writing makes the book a quick read.'
      Norman M. Goldfarb for Journal of Clinical Research Best Practices, Vol. 13, No. 12, December 2017.



      Table of Contents

      Chapter 1: Rules, Roles and Responsibilities

      Chapter 2: Products, Protocols, and Pre-trial Preparation

      Chapter 3: Sponsor, Site and Study Start-up

      Chapter 4: Enticement, Enrollment, and Engagement: The Informed Consent Process

      Chapter 5: From Enrollment to Final Visit

      Chapter 6: Collaborating for Compliance and Quality Data – Monitoring and Audits

      Chapter 7: Building Budgets

      Chapter 8: Contracts, Clauses and Closing the Deal

      Chapter 9: US Clinical Trials – Additional Topics

      Chapter 10: Clinical Research and India

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