Description

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

The Coordination of Clinical Research

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RRP: £85.50 You save £8.55 (10%)
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by Mohit Bhandari

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Short Description:

A novel and indispensable handbook for clinical research coordinators worldwideBecause saying isn''t doing; doing is doing: This fourth volume in... Read more

    Publisher: Thieme Publishing Group
    Publication Date: 1/24/2020
    ISBN13: 9783132422292, 978-3132422292
    ISBN10: 3132422290

    Non Fiction , Education

    Description

    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

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