Overview

A novel and indispensable handbook for clinical research coordinators worldwide Because saying isn't doing; doing is doing : This fourth volume in Mohit Bhandari's 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.

Full Product Details

Author:   Mohit Bhandari ,  Esther Van Lieshout
Publisher:   Thieme Publishing Group
Imprint:   Thieme Publishing Group
Weight:   0.813kg
ISBN:  

9783132422292

ISBN 10:   3132422290
Pages:   340
Publication Date:   24 January 2020
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Mixed media product
Publisher's Status:   Active
Availability:   Out of stock  
The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available.

Table of Contents

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 Coordinator's 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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