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Literature DB >> 12497701

The invisible hand in clinical research: the study coordinator's critical role in human subjects protection.

Arlene M Davis¹, Sara Chandros Hull, Christine Grady, Benjamin S Wilfond, Gail E Henderson.

Abstract

Entities: Species

Keywords: Biomedical and Behavioral Research; Empirical Approach; University of North Carolina School of Medicine; Warren G. Magnuson Clinical Center (National Institutes of Health)

Mesh：

Year: 2002 PMID： 12497701 PMCID： PMC4819323 DOI： 10.1111/j.1748-720x.2002.tb00410.x

Source DB: PubMed Journal: J Law Med Ethics ISSN： 1073-1105 Impact factor: 1.718

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19 in total

1. Reforming informed consent to genetic research.

Authors: G J Annas
Journal: JAMA Date: 2001-11-14 Impact factor: 56.272

2. The globalization of clinical trials: a growing challenge in protecting human subjects: executive summary (2001).

Authors:
Journal: J Int Bioethique Date: 2003 Mar-Jun

3. My role as research nurse coordinator.

Authors: D A Seguin
Journal: Crit Care Nurs Q Date: 1990-03

4. Ethical issues in clinical trials.

Authors: C Grady
Journal: Semin Oncol Nurs Date: 1991-11 Impact factor: 2.315

5. Nurse researcher: a study of a contradiction in terms?

Authors: C Hicks
Journal: J Adv Nurs Date: 1996-08 Impact factor: 3.187

6. Establishing a research coordinator network: the birth of an idea.

Authors: D J Ecklund
Journal: J Nurs Adm Date: 1999-01 Impact factor: 1.737

7. Subject retention in a controlled clinical trial.

Authors: M Good; L Schuler
Journal: J Adv Nurs Date: 1997-08 Impact factor: 3.187

8. Effect of a research nurse on patient enrollment in a clinical study.

Authors: D J Isaacman; E A Reynolds
Journal: Pediatr Emerg Care Date: 1996-10 Impact factor: 1.454

9. Conflict of interest and the physician-researcher.

Authors: M L Elks
Journal: J Lab Clin Med Date: 1995-07

10. Physician-investigator/patient-subject: exploring the logic and the tension.

Authors: L R Churchill
Journal: J Med Philos Date: 1980-09

34 in total

1. Evolution of the study coordinator role: the 28-year experience in Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC).

Authors: Mary E Larkin; Gayle M Lorenzi; Meg Bayless; Patricia A Cleary; Annette Barnie; Ellen Golden; Susan Hitt; Saul Genuth
Journal: Clin Trials Date: 2012-06-22 Impact factor: 2.486

2. Co-ordinating 'ethical' clinical trials: the role of research coordinators in the contract research industry.

Authors: Jill A Fisher
Journal: Sociol Health Illn Date: 2006-09

3. How do clinical research coordinators learn Good Clinical Practice? A mixed-methods study of factors that predict uptake of knowledge.

Authors: Jessica T Mozersky; Alison L Antes; Kari Baldwin; Michelle Jenkerson; James M DuBois
Journal: Clin Trials Date: 2020-01-27 Impact factor: 2.486

The invisible hand in clinical research: the study coordinator's critical role in human subjects protection.

1. Reforming informed consent to genetic research.

2. The globalization of clinical trials: a growing challenge in protecting human subjects: executive summary (2001).

3. My role as research nurse coordinator.

4. Ethical issues in clinical trials.

5. Nurse researcher: a study of a contradiction in terms?

6. Establishing a research coordinator network: the birth of an idea.

7. Subject retention in a controlled clinical trial.

8. Effect of a research nurse on patient enrollment in a clinical study.

9. Conflict of interest and the physician-researcher.

10. Physician-investigator/patient-subject: exploring the logic and the tension.

1. Evolution of the study coordinator role: the 28-year experience in Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC).

2. Co-ordinating 'ethical' clinical trials: the role of research coordinators in the contract research industry.

3. How do clinical research coordinators learn Good Clinical Practice? A mixed-methods study of factors that predict uptake of knowledge.

4. Bridging the Researcher-Participant Gap: A Research Agenda to Build Effective Research Relationships.

5. A CTSA-sponsored program for clinical research coordination: networking, education, and mentoring.

6. Precluding consent by clinicians who are both the attending and the investigator: an outdated shibboleth?

7. "Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.

8. NETT coordinators: researchers, caregivers, or both?

9. Practicing research ethics: private-sector physicians & pharmaceutical clinical trials.

10. Role of clinical research coordinators in promoting clinical trials of drugs for surgical patients.