The Comprehensive Guide To Clinical Research
The Comprehensive Guide To Clinical Research

Author: Chris Sauber

Publisher: Independently Published

Published: 2019-04-21

Total Pages: 218

ISBN-13: 9781090349521

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Condensing the most important topics in all of clinical research in an easy to understand presentation. The 20 percent of what you need to know in order to be 80 percent proficient!The authors who have operated various levels of businesses in the clinical research industry since 2005 believe that more practical information pertaining to clinical research needs to be accessible to individuals who are new to the industry or are curious about entering the rewarding world of clinical trials.This book reads in an easy to understand style and is based on proven methods the authors have developed to train their own employees and students of their various clinical research academies throughout the years. Picking this up and absorbing the information will allow anyone to gain much better insight into the complicated dynamics of clinical research. This practical roadmap is all you will need to get started on your clinical trial journey!In this book you will learn about:Regulations and the history as well as evolution of GCP.Clinical Research Site OperationsMonitoring Dynamics and Typical Monitoring VistsCRO ActivitiesSponsor Level DynamicsIndustry VendorsCommon Career Opportunities and Employment Roadmaps

Career Opportunities in Clinical Drug Research
Career Opportunities in Clinical Drug Research

Author: Rebecca Jane Anderson

Publisher: Rebecca Anderson

Published: 2010

Total Pages: 288

ISBN-13: 1936113058

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"It is simply amazing to me that so many of my industry coworkers stumbled upon their careers in clinical research, like I did, merely by chance. In most cases, once those opportunities were presented to us, we found fulfilling and successful careers. Undoubtedly, other eager job seekers would also find this career path attractive. If only someone would tell them about it."

Get A Job As A Clinical Research Associate
Get A Job As A Clinical Research Associate

Author: Lasonya Dembek

Publisher:

Published: 2021-07-25

Total Pages: 26

ISBN-13:

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A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a healthcare professional who performs many activities related to medical research, particularly clinical trials. Whilst there is a wealth of information on clinical research available to those willing to investigate, knowing where to start can be a daunting prospect for the uninitiated. This guide was developed out of the author's recent work mentoring new graduates. The aim of this guide is to provide the reader with a sound understanding of the day-to-day aspects of the role, thereby enabling them to plan a suitable career path accordingly

Become A Clinical Research Associate
Become A Clinical Research Associate

Author: Janee Lacrue

Publisher:

Published: 2021-07-25

Total Pages: 26

ISBN-13:

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A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a healthcare professional who performs many activities related to medical research, particularly clinical trials. Whilst there is a wealth of information on clinical research available to those willing to investigate, knowing where to start can be a daunting prospect for the uninitiated. This guide was developed out of the author's recent work mentoring new graduates. The aim of this guide is to provide the reader with a sound understanding of the day-to-day aspects of the role, thereby enabling them to plan a suitable career path accordingly

Principles and Practice of Clinical Research
Principles and Practice of Clinical Research

Author: John I. Gallin

Publisher: Elsevier

Published: 2011-04-28

Total Pages: 447

ISBN-13: 0080489567

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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

The CRC's Guide to Coordinating Clinical Research
The CRC's Guide to Coordinating Clinical Research

Author: Karen E. Woodin

Publisher: CenterWatch

Published: 2004

Total Pages: 428

ISBN-13:

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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.

Clinical Research Coordinator Handbook
Clinical Research Coordinator Handbook

Author: Deborrah Norris

Publisher: Plexus Publishing (UK)

Published: 2004

Total Pages: 164

ISBN-13:

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In this revised third edition of the essential reference for clinical research coordinators (CRCs), Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The book's five appendices include a directory of CRC resources, updated forms and checklists, state regulatory requirements and contact information, conversion charts and tables, a glossary, and more.

Economic Evaluation in Clinical Trials
Economic Evaluation in Clinical Trials

Author: Henry A. Glick

Publisher: OUP Oxford

Published: 2014-10-02

Total Pages: 265

ISBN-13: 0191508055

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It is becoming increasingly important to examine the relationship between the outcomes of a clinical trial and the costs of the medical therapy under study. The results of such analysis can affect reimbursement decisions for new medical technologies, drugs, devices or diagnostics. It can aid companies seeking to make claims about the cost-effectiveness of their product, as well as allowing early consideration of the economic value of therapies which may be important to improving initial adoption decisions. It is also vital for addressing the requirements of regulatory bodies. Economic Evaluation in Clinical Trials provides practical advice on how to conduct cost-effectiveness analyses in controlled trials of medical therapies. This new edition has been extensively rewritten and revised; topics discussed range from design issues such as the types of services that should be measured and price weights, to assessment of quality-adjusted life years. Illustrative materials, case histories and worked examples are included to encourage the reader to apply the methods discussed. These exercises are supported with datasets, programmes and solutions made available online.

Careers with the Pharmaceutical Industry
Careers with the Pharmaceutical Industry

Author: Peter D. Stonier

Publisher: John Wiley & Sons

Published: 2003-05-07

Total Pages: 380

ISBN-13: 9780470843284

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In recent years, many factors have combined to change the operating environment of the international pharmaceutical industry leading to greater specialisation and sophistication. This new edition will give an update of the different opportunities in drug discovery and development and the scientific, medical or other specialist training needed to accomplish them. The scope of this edition has been broadened to encompass all major roles, including marketing and sales.