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The Coordination of Clinical Research

A Handbook for Research Coordinators. Plus Online at MedOne - Paperback (Thread Stitching)
BundleNon-Book
340 Seiten
Englisch
Thiemeerschienen am24.01.2020
A novel and indispensable handbook for clinical research coordinators worldwideBecause "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 experienceIncludes 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 moreMany helpful templates and sample forms with checklists, consent forms, budget outlines, and moreA 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.mehr
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E-BookPDF1 - PDF WatermarkE-Book
EUR99,99
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BundleNon-Book
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Produkt

KlappentextA novel and indispensable handbook for clinical research coordinators worldwideBecause "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 experienceIncludes 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 moreMany helpful templates and sample forms with checklists, consent forms, budget outlines, and moreA 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.
Details
ISBN/GTIN978-3-13-242229-2
ProduktartBundle
EinbandartNon-Book
Verlag
Erscheinungsjahr2020
Erscheinungsdatum24.01.2020
Seiten340 Seiten
SpracheEnglisch
Gewicht813 g
Illustrationen35 Abb.
Artikel-Nr.47817816
Rubriken
GenreMedizin

Inhalt/Kritik

Inhaltsverzeichnis
Part I Getting Started1 Leadership and Management: The Principal Investigator and Research Coordinator2 Roles: Why a Research Coordinator is Critical3 Hiring: Characteristics of a Highly Qualified Research Coordinator4 Growth: From 0 to 100, Real Quick!Part II What Every Research Coordinator Needs to Know5 What is Evidence-Based Medicine?6 Randomized Controlled Trials7 Observational Studies8 Surveys9 Qualitative Studies10 Principles of Good Clinical Practice and Research ConductPart III From Idea to Study Start-Up11 Principles of Grant Writing: Tips for a Successful Experience12 Dollars and "Sense": A Guide to Research Finances13 Maintaining Records and the Trial Master File14 Ethics Submissions15 The Basics of Research Contracts16 How to Start-Up a StudyPart IV Study Execution and Close-Out17 Screening and Recruiting Participants18 Obtaining Informed Consent19 Collecting Data: Paper and Electronic Data Capture Systems20 Follow-Up: Why It Is Important and How to Minimize Loss to Follow-Up21 How to Close Out a Study22 Knowledge Dissemination: Getting the Word Out!Part V Advanced Principles of Research Coordination23 Regulatory Trials: Key Differences from Standard Trials24 How to Survive a Site Audit25 Monitoring in a Clinical Study: Why and How?26 Managing Large Studies: Organization and Committees27 International Research: Challenges and SuccessesPart VI A Coordinator's ToolboxToolbox AToolbox BToolbox CToolbox DToolbox EToolbox F1Toolbox F2Toolbox F3Toolbox F4Toolbox F5Toolbox F6Toolbox F7Toolbox F8Toolbox F9Toolbox F10Toolbox F11Toolbox Gmehr