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The Coordination of Clinical Research: A Handbook for Research Coordinators

The Coordination of Clinical Research: A Handbook for Research Coordinators

9783132422292
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Description

A novel and indispensable handbook for clinical research coordinators worldwide

Because saying isnt doing; doing is doing:: This fourth volume in Mohit Bhandaris series of methodology books, conceived as a transformational guide to executing research for those who coordinate it on a daily basis, focuses not on the design of research projects, but rather on the actual execution of such projects.

Key Features::

  • International group of authors and practicing research coordinators with decades of collective hands-on experience
  • Includes many crucial, but often neglected, topics such as principles of successful grant writing, working with study budgets, ethics and consent forms, regulatory versus standard trials, coordinating and conducting observational research and randomized clinical trials, and much more
  • Many helpful templates and sample forms with checklists, consent forms, budget outlines, and more

A broad readership including scientists, physicians, surgeons, epidemiologists and statisticians, and industry research and development directors will welcome this unique and valuable book.

This book includes complimentary access to a digital copy on https:://medone.thieme.com.

Product Details
Georg Thieme
81882
9783132422292
9783132422292

Data sheet

Publication date
2020
Issue number
1
Cover
paperback
Pages count
340
Dimensions (mm)
175.26 x 241.94
Weight (g)
813

  • Part I Getting Started
    1 Leadership and Management: The Principal Investigator and Research Coordinator
    2 Roles: Why a Research Coordinator is Critical
    3 Hiring: Characteristics of a Highly Qualified Research Coordinator
    4 Growth: From 0 to 100, Real Quick!
    Part II What Every Research Coordinator Needs to Know
    5 What is Evidence-Based Medicine?
    6 Randomized Controlled Trials
    7 Observational Studies
    8 Surveys
    9 Qualitative Studies
    10 Principles of Good Clinical Practice and Research Conduct
    Part III From Idea to Study Start-Up
    11 Principles of Grant Writing: Tips for a Successful Experience
    12 Dollars and Sense: A Guide to Research Finances
    13 Maintaining Records and the Trial Master File
    14 Ethics Submissions
    15 The Basics of Research Contracts
    16 How to Start-Up a Study
    Part IV Study Execution and Close-Out
    17 Screening and Recruiting Participants
    18 Obtaining Informed Consent
    19 Collecting Data: Paper and Electronic Data Capture Systems
    20 Follow-Up: Why It Is Important and How to Minimize Loss to Follow-Up
    21 How to Close Out a Study
    22 Knowledge Dissemination: Getting the Word Out!
    Part V Advanced Principles of Research Coordination
    23 Regulatory Trials: Key Differences from Standard Trials
    24 How to Survive a Site Audit
    25 Monitoring in a Clinical Study: Why and How?
    26 Managing Large Studies: Organization and Committees
    27 International Research: Challenges and Successes
    Part VI A Coordinators Toolbox
    Toolbox A
    Toolbox B
    Toolbox C
    Toolbox D
    Toolbox E
    Toolbox F1
    Toolbox F2
    Toolbox F3
    Toolbox F4
    Toolbox F5
    Toolbox F6
    Toolbox F7
    Toolbox F8
    Toolbox F9
    Toolbox F10
    Toolbox F11
    Toolbox G

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