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Download or read book The CRC's Guide to Coordinating Clinical Research written by Sather and published by . This book was released on 2016-05-20 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author: SANDRA. SATHER
Publisher:
Published: 2015
Total Pages:
ISBN-13: 9781604301007
DOWNLOAD EBOOKDownload or read book THE CRCS GUIDE TO COORDINATING CLINICAL RESEARCH,FOURTH EDITION. written by SANDRA. SATHER and published by . This book was released on 2015 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author: Karen E. Woodin
Publisher:
Published: 2011-06
Total Pages: 573
ISBN-13: 9781930624610
DOWNLOAD EBOOKNew chapters, updated content, more tips, helpful exercises and more! The CRC's Guide to Coordinating Clinical Research has been one of the foremost training tools and reference guides for novice and experienced coordinators since the first edition was released in 2004. Now with new chapters on investigational product accountability, device and biologics trials and data safety monitoring boards, along with key takeaways and newly added case studies, The CRC's Guide is the most comprehensive resource available for on-site training staffs, professors or individuals interested in a step-by-step approach to coordinating successful clinical trials. Topics include: A comprehensive review of CRC roles and responsibilities Understanding regulations and GCPs Preparing for a study Working with study subjects The informed consent process Case report forms and EDC Study closure The future outlook Job descriptions and current academic programs Adverse Events and Safety Monitoring Sample Forms, Checklists and Logs Recommended for: Novice and experienced CRCs Health professionals interested in pursuing a career as a study coordinator Instructors conducting training and educational programs
Download or read book The CRC's Guide to Coordinating Clinical Research written by Karen E. Woodin and published by . This book was released on 2011-06 with total page 573 pages. Available in PDF, EPUB and Kindle. Book excerpt: New chapters, updated content, more tips, helpful exercises and more! The CRC's Guide to Coordinating Clinical Research has been one of the foremost training tools and reference guides for novice and experienced coordinators since the first edition was released in 2004. Now with new chapters on investigational product accountability, device and biologics trials and data safety monitoring boards, along with key takeaways and newly added case studies, The CRC's Guide is the most comprehensive resource available for on-site training staffs, professors or individuals interested in a step-by-step approach to coordinating successful clinical trials. Topics include: A comprehensive review of CRC roles and responsibilities Understanding regulations and GCPs Preparing for a study Working with study subjects The informed consent process Case report forms and EDC Study closure The future outlook Job descriptions and current academic programs Adverse Events and Safety Monitoring Sample Forms, Checklists and Logs Recommended for: Novice and experienced CRCs Health professionals interested in pursuing a career as a study coordinator Instructors conducting training and educational programs
Author: Kane Williams
Publisher: Createspace Independent Publishing Platform
Published: 2017-05-15
Total Pages: 234
ISBN-13: 9781546939658
DOWNLOAD EBOOKThis 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.
Download or read book Clinical Research Coordinator Manual written by Kane Williams and published by Createspace Independent Publishing Platform. This book was released on 2017-05-15 with total page 234 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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: Karen E. Woodin
Publisher: CenterWatch
Published: 2004
Total Pages: 428
ISBN-13:
DOWNLOAD EBOOKThis guidebook is filled with valuable information on the role and responsibilities of a clinical research coordinator (CRC) and explains the research process from the site and CRC perspective. Topics covered include: identifying the regulations governing clinical research; describing the drug development process; discussing good clinical practices and how to apply them in clinical trials and organizing a clinical practice.
Download or read book The CRC's Guide to Coordinating Clinical Research written by Karen E. Woodin and published by CenterWatch. This book was released on 2004 with total page 428 pages. Available in PDF, EPUB and Kindle. Book excerpt: This guidebook is filled with valuable information on the role and responsibilities of a clinical research coordinator (CRC) and explains the research process from the site and CRC perspective. Topics covered include: identifying the regulations governing clinical research; describing the drug development process; discussing good clinical practices and how to apply them in clinical trials and organizing a clinical practice.
Author: Kane Williams
Publisher:
Published: 2017-05-15
Total Pages: 234
ISBN-13: 9781546916833
DOWNLOAD EBOOKThis 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.
Download or read book Clinical Research Coordinator?s Manual written by Kane Williams and published by . This book was released on 2017-05-15 with total page 234 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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: Deena Bernstein
Publisher:
Published: 2015-06-01
Total Pages:
ISBN-13: 9780988193857
DOWNLOAD EBOOKCITI Progam's Clinical Research Coordinator (CRC) Guide provides clinical research professionals with information on operational and regulatory elements necessary for the ethical conduct of clinical trials. Information presented in this guide expands beyond but is directly connected to elements of Human Subjects Research (HSR) and Good Clinical Practice (GCP). Readers may find this guide most helpful if they have an understanding of these areas, as it will provide a foundation for many of concepts, ideas, and considerations presented.Each chapter consists of foundational text, supplemented by a number of case studies and resources, which are intended to help readers conceptualize and establish a greater understanding of the topic being discussed. Readers seeking further resources may access a resource database for clinical research professionals by signing up for the CITI Program's online CRC course. The resource database (presented as a module) outlines and provides links to various tools such as job aids, templates, reporting forms and guidance, FDA forms, best practices, federal regulations, international resources, ethical codes, and more.It is our hope that the content presented within this guide is operational in nature and will empower readers to perform their roles in clinical research efficiently and with confidence. This paperback edition is exclusively available at https://www.citiprogram.org/publications
Download or read book Clinical Research Coordinator (CRC) Guide written by Deena Bernstein and published by . This book was released on 2015-06-01 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: CITI Progam's Clinical Research Coordinator (CRC) Guide provides clinical research professionals with information on operational and regulatory elements necessary for the ethical conduct of clinical trials. Information presented in this guide expands beyond but is directly connected to elements of Human Subjects Research (HSR) and Good Clinical Practice (GCP). Readers may find this guide most helpful if they have an understanding of these areas, as it will provide a foundation for many of concepts, ideas, and considerations presented.Each chapter consists of foundational text, supplemented by a number of case studies and resources, which are intended to help readers conceptualize and establish a greater understanding of the topic being discussed. Readers seeking further resources may access a resource database for clinical research professionals by signing up for the CITI Program's online CRC course. The resource database (presented as a module) outlines and provides links to various tools such as job aids, templates, reporting forms and guidance, FDA forms, best practices, federal regulations, international resources, ethical codes, and more.It is our hope that the content presented within this guide is operational in nature and will empower readers to perform their roles in clinical research efficiently and with confidence. This paperback edition is exclusively available at https://www.citiprogram.org/publications
Download or read book The CRCþs Guide to Coordinating Clinical Research written by Karen E. Woodin and published by . This book was released on 2004 with total page 411 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author: Clinical Research Association (LONDON)
Publisher:
Published: 1935
Total Pages: 230
ISBN-13:
DOWNLOAD EBOOKDownload or read book The Practitioner's Guide to Clinical Research. Fourth Edition, Etc. [With Plates.]. written by Clinical Research Association (LONDON) and published by . This book was released on 1935 with total page 230 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author: John I. Gallin
Publisher: Elsevier
Published: 2011-04-28
Total Pages: 447
ISBN-13: 0080489567
DOWNLOAD EBOOKThe second edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research. Molecular medicine, genomics, and proteomics have opened vast opportunities for translation of basic science observations to the bedside through clinical research. As an introductory reference it gives clinical investigators in all fields an awareness of the tools required to ensure research protocols are well designed and comply with the rigorous regulatory requirements necessary to maximize the safety of research subjects. Complete with sections on the history of clinical research and ethics, copious figures and charts, and sample documents it serves as an excellent companion text for any course on clinical research and as a must-have reference for seasoned researchers. *Incorporates new chapters on Managing Conflicts of Interest in Human Subjects Research, Clinical Research from the Patient's Perspective, The Clinical Researcher and the Media, Data Management in Clinical Research, Evaluation of a Protocol Budget, Clinical Research from the Industry Perspective, and Genetics in Clinical Research *Addresses the vast opportunities for translation of basic science observations to the bedside through clinical research*Delves into data management and addresses how to collect data and use it for discovery*Contains valuable, up-to-date information on how to obtain funding from the federal government
Download or read book Principles and Practice of Clinical Research written by John I. Gallin and published by Elsevier. This book was released on 2011-04-28 with total page 447 pages. Available in PDF, EPUB and Kindle. Book excerpt: The second edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research. Molecular medicine, genomics, and proteomics have opened vast opportunities for translation of basic science observations to the bedside through clinical research. As an introductory reference it gives clinical investigators in all fields an awareness of the tools required to ensure research protocols are well designed and comply with the rigorous regulatory requirements necessary to maximize the safety of research subjects. Complete with sections on the history of clinical research and ethics, copious figures and charts, and sample documents it serves as an excellent companion text for any course on clinical research and as a must-have reference for seasoned researchers. *Incorporates new chapters on Managing Conflicts of Interest in Human Subjects Research, Clinical Research from the Patient's Perspective, The Clinical Researcher and the Media, Data Management in Clinical Research, Evaluation of a Protocol Budget, Clinical Research from the Industry Perspective, and Genetics in Clinical Research *Addresses the vast opportunities for translation of basic science observations to the bedside through clinical research*Delves into data management and addresses how to collect data and use it for discovery*Contains valuable, up-to-date information on how to obtain funding from the federal government
