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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RRP £91.99 – you save £4.60 (5%)

Order before 4pm today for delivery by Thu 18 Dec 2025.

A Hardback by JoAnn Pfeiffer, Cris Wells

1 in stock


    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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