Principles and Practice of Clinical Research
Academic Press Inc (Verlag)
978-0-12-849905-4 (ISBN)
In addition to key topics such as bioethics, clinical outcome data, cultural diversity, protocol guidelines, and “omic platforms, this edition contains new chapters devoted to electronic health records and information resources for clinical researchers, as well as the many opportunities associated with big data. Covering a vast number of topics and practical advice for both novice and advanced clinical investigators, this book is a highly relevant and essential resource for all those involved in conducting research.
Dr. John Gallin was appointed to the dual roles of National Institutes of Health (NIH) Associate Director for Clinical Research and inaugural Chief Scientific Officer, the Clinical Center in August 2016. He served as the Director NIH Clinical Center from 1994-2017 after serving 9 years as Scientific Director of the National Institute of Allergy and Infectious Diseases (NIAID) and 12 years as Chief of the Laboratory of Host Defenses. During his tenure as Director of the NIH Clinical Center, Dr. Gallin helped to lead the design, construction, and activation of the Mark O. Hatfield Clinical Research Center, the largest hospital in the world totally dedicated to clinical research. He also oversaw the establishment of a new curriculum for clinical research training, now offered globally reaching over 25,000 students annually in 168 countries, and the development of new information systems for biomedical, translational and clinical research. In 2011, Dr. Gallin accepted, on behalf of the NIH Clinical Center, the Lasker–Bloomberg Public Service Award for its rich history of medical discovery through clinical research. His primary research interests are rare immune disorders of phagocytes, with a focus on chronic granulomatous disease (CGD). His laboratory described the genetic basis for several forms of CGD and other disorders of phagocytes and has done pioneering research that has reduced life-threatening bacterial and fungal infections in patients with these disorders. He has published more than 380 articles in scientific journals and edited two textbooks – Inflammation, Basic Principles and Clinical Correlates (Lippincott, Williams, and Wilkins, 1999, 3rd edition) and Principles and Practice of Clinical Research (Academic Press, 4th edition 2018). He has received numerous awards and honors for his accomplishments and in 2022 received the Weill Cornell Medical College Alumni Award of Distinction, the medical college’s most prestigious alumni award. Dr. Gallin is a member of the American Society for Clinical Investigation, the Association of American Physicians, the National Academy of Medicine of the National Academy of Sciences, a Master of the American College of Physicians, and a Fellow of the Royal College of Physicians-London. He retired from his administrative positions in 2023 and is now an Adjunct Senior Investigator at NIH in the Laboratory of Clinical Immunology and Microbiology in the National Institute of Allergy and Infectious Diseases. Laura Lee Johnson, Ph.D. is the patient focused drug development liaison and the division director for the Office of Biostatistics at the U.S. Food and Drug Administration (FDA) Center for Drug Evaluation and Research (CDER). She specializes in design, logistics, implementation, and analysis of research studies of all sizes and in measurement tool and endpoint development. Prior to working at the FDA she spent over a decade at the U.S. National Institutes of Health working on and overseeing clinical research and research support programs.
1. A Historical Perspective on Clinical Research
Part I - Ethical, Regulatory and Legal Issues
2. Ethical Principles in Clinical Research
3. Integrity in Research: Principles for the Conduct of Research
4. Institutional Review Boards
5. The Regulation of Drugs and Biological Products by the Food and Drug Administration
6. International Regulation of Drugs and Biological Products
7. Data Management in Clinical Trials
8. Data and Safety Monitoring
9. Unanticipated Risk in Clinical Research
10. Legal Issues
11. Inclusion of Women and Minorities as Subjects in Clinical Research
12. Accreditation of Human Research Protection Programs
13. The Role and Importance of Clinical Trials Registries
14. The Clinical Researcher and the Media
15. Clinical Research: A Patient Perspective
Part II - Biostatistics and Epidemiology
16. Design of Observational Studies
17. Design of Interventional Studies and Trials
18. Issues in Randomization
19. Hypothesis Testing
20. Power and Sample Size Calculations
21. An Introduction to Survival Analysis
22. Intermediate Topics in Biostatistics
23. Measures of Function and Health-Related Quality of Life
24. Large Clinical Trials and Registries: Clinical Research Institutes
25. Meta-analysis of Clinical Trials
26. Using Large Datasets for Population-based Health Research
27. Development and Conduct of Studies
Part III - Technology Transfer, Protocol Development, and Sources of Funding Support for Research
28. Overview of Technology Development and Technology Transfer
29. Writing a Protocol
30. Evaluating a Protocol Budget
31. Clinical Research Data: Characteristics, Representation, Storage and Retrieval
32. Management of Patient Samples and Specimens
33. Getting the Funding You Need to Support Your Research: Navigating the National Institutes of Health Peer Review Process
34. Clinical Research from the Industry Perspective
35. Philanthropy's Role in Advancing Biomedical Research
Part IV - Clinical Research Infrastructure
36. Managing Clinical Risk and Measuring Participants’ Perceptions of the Clinical Research Process
37. Clinical Pharmacology and its Role in Pharmaceutical Development
38. Career Paths in Clinical Research
39. Clinical Research Nursing: A New Domain of Practice
40. Issues and Challenges for Clinical Research in International Settings
41. The Role of Comparative Effectiveness Research
42. The Importance and Use of Electronic Health Records in Clinical Research
43. Informational Resources for the Clinical Researcher
| Erscheinungsdatum | 22.01.2018 |
|---|---|
| Verlagsort | San Diego |
| Sprache | englisch |
| Maße | 216 x 276 mm |
| Gewicht | 2360 g |
| Themenwelt | Medizinische Fachgebiete ► Innere Medizin ► Endokrinologie |
| ISBN-10 | 0-12-849905-2 / 0128499052 |
| ISBN-13 | 978-0-12-849905-4 / 9780128499054 |
| Zustand | Neuware |
| Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
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