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Author: Susan L. Copp Publisher: ISBN: Category : Medical research personnel Languages : en Pages : 404
Book Description
Three learning modules were developed for the on-line orientation manual: (1) An Overview of Clinical Research, (2) Roles and Responsibilities of Clinical Research Coordinators, and (3) a Research Glossary. Each module provides the research coordinator with background information, access to outside websites, and specific examples related to the conduct of clinical research at the site. The on-line orientation provides consistency in educating the new coordinator and enables the new clinical research coordinator to learn, integrate, and apply knowledge to the work setting.
Author: Susan L. Copp Publisher: ISBN: Category : Medical research personnel Languages : en Pages : 404
Book Description
Three learning modules were developed for the on-line orientation manual: (1) An Overview of Clinical Research, (2) Roles and Responsibilities of Clinical Research Coordinators, and (3) a Research Glossary. Each module provides the research coordinator with background information, access to outside websites, and specific examples related to the conduct of clinical research at the site. The on-line orientation provides consistency in educating the new coordinator and enables the new clinical research coordinator to learn, integrate, and apply knowledge to the work setting.
Author: Mohit Bhandari Publisher: Thieme ISBN: 3132582549 Category : Medical Languages : en Pages : 505
Book 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 A broad readership including scientists, physicians, surgeons, epidemiologists and statisticians, and industry research and development directors will welcome this unique and valuable book.
Author: Kane Williams Publisher: Createspace Independent Publishing Platform ISBN: 9781546939658 Category : Clinical trials Languages : en Pages : 234
Book Description
This book is divided into 25 chapters covering more than 300 topics. This book will serve as a training guide to make your routine tasks more efficient, compliant and easy. After reading this book, Clinical Research Coordinators, clinical research personnel and aspirants would get: # Step by step in-depth training on roles and responsibilities of a clinical research coordinator before, during and after the completion of a clinical trial. # Discussion on day-to-day challenges and their solutions. # Training through real-time examples and ready-made checklists to conduct each activity more efficiently and correctly. # Guidance through strategies and measures to execute critical clinical trial activities. # Training on regulatory and ICH-GCP guidelines. # Tips on effective communication and coordination with site staff, investigator, sponsor, and IRB. # Assistance to become a better and successful clinical research coordinator. # Knowledge on other essential topics of clinical research.
Author: JoAnn Pfeiffer Publisher: CRC Press ISBN: 1315299771 Category : Mathematics Languages : en Pages : 292
Book Description
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 growing market of Indian clinical trials.
Author: Kane Williams Publisher: ISBN: 9781546916833 Category : Languages : en Pages : 234
Book Description
This book is divided into 25 chapters covering more than 300 topics. This book will serve as a training guide to make your routine tasks more efficient, compliant and easy. After reading this book, Clinical Research Coordinators, clinical research personnel and aspirants would get:# Step by step in-depth training on roles and responsibilities of a clinical research coordinator before, during and after the completion of a clinical trial.# Discussion on day-to-day challenges and their solutions.# Training through real-time examples and ready-made checklists to conduct each activity more efficiently and correctly.# Guidance through strategies and measures to execute critical clinical trial activities.# Training on regulatory and ICH-GCP guidelines.# Tips on effective communication and coordination with site staff, investigator, sponsor, and IRB.# Assistance to become a better and successful clinical research coordinator. # Knowledge on other essential topics of clinical research.
Author: Jan Van den Akker Publisher: Routledge ISBN: 1134155654 Category : Education Languages : en Pages : 177
Book Description
The field of design research has been gaining momentum over the last five years, particularly in educational studies. As papers and articles have grown in number, definition of the domain is now beginning to standardise. This book fulfils a growing need by providing a synthesised assessment of the use of development research in education. It looks at four main elements: background information including origins, definitions of development research, description of applications and benefits and risks associated with studies of this kind how the approach can serve the design of learning environments and educational technology quality assurance - how to safeguard academic rigor while conducting design and development studies a synthesis and overview of the topic along with relevant reflections.
Author: Institute of Medicine Publisher: National Academies Press ISBN: 0309253187 Category : Medical Languages : en Pages : 248
Book Description
There is growing recognition that the United States' clinical trials enterprise (CTE) faces great challenges. There is a gap between what is desired - where medical care is provided solely based on high quality evidence - and the reality - where there is limited capacity to generate timely and practical evidence for drug development and to support medical treatment decisions. With the need for transforming the CTE in the U.S. becoming more pressing, the IOM Forum on Drug Discovery, Development, and Translation held a two-day workshop in November 2011, bringing together leaders in research and health care. The workshop focused on how to transform the CTE and discussed a vision to make the enterprise more efficient, effective, and fully integrated into the health care system. Key issue areas addressed at the workshop included: the development of a robust clinical trials workforce, the alignment of cultural and financial incentives for clinical trials, and the creation of a sustainable infrastructure to support a transformed CTE. This document summarizes the workshop.
Author: Susan L. Copp
Author: Susan L. Copp
Author: Mohit Bhandari
Author: Kane Williams
Author: JoAnn Pfeiffer
Author: Kane Williams
Author: 
Author: Jan Van den Akker
Author: National Library of Medicine (U.S.)
Author: Educational Resources Information Center (U.S.)
Author: Institute of Medicine