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Clinical research coordinator
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491	Japan’s Regulatory Initiative to promote Global Clinical Development Shinobu UZU International Planning Director, Ministers’ Secreatriat, MHLW Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2010-10-20 06:13:55 Health Science Medical statistics Health research Food and Drug Administration Clinical trial Medical research ClinicalTrials.gov Clinical research coordinator Clinical research Research Pharmaceutical industry
492	APPENDIX VI AN AID TO CONSTRUCTING AN INFORMATION/CONSENT FORM For therapeutic interventions or drug trials. IMPORTANT: It is recommended that the information sheet and consent form be combined into one form. Add to Reading List Source URL: www.queensu.ca Language: English - Date: 2014-10-31 15:21:26 Research Pharmacology Medical ethics Design of experiments Bioethics Clinical trial Placebo Clinical research coordinator Randomized controlled trial Clinical research Medicine Science
493	Institutional Review Board & Human Subjects Office Back to School Reminder As student investigators return to classes this spring semester, the Human Subjects Office (HSO) would like to offer a friendly reminder to those Add to Reading List Source URL: hso.research.uiowa.edu Language: English - Date: 2014-01-23 09:04:45 Science Institutional review board Grant Human subject research Clinical research coordinator Ethical research in social science Clinical research Research Ethics
494	ANDS Guides – Awareness level Research data policy and the Australian Code for the Responsible Conduct of Research Who should read this? This guide is designed as an introduction for academic administrators who have r Add to Reading List Source URL: www.ands.org.au Language: English - Date: 2014-09-22 21:25:32 Data sharing Environmental science Scientific method Scientific misconduct Business Records management Environment Data management plan Clinical research coordinator Science Information technology management Climatology
495	Institutional Review Board & Human Subjects Office Faculty Advisor Oversight Responsibilities and Assurances Purpose The Faculty Advisor listed on a HawkIRB application must be a member of the University of Iowa faculty Add to Reading List Source URL: hso.research.uiowa.edu Language: English - Date: 2014-01-22 17:54:31 Pharmacology Scientific method Drug safety Science Institutional review board Public Responsibility in Medicine and Research Clinical research coordinator Ethical research in social science Clinical research Research Design of experiments
496	PERMISSION ONTOLOGY FOR REUSING AND SHARING BIO-SAMPLES AND DATA OBTAINED FROM INFORMED CONSENT Maria Adela Grando, PhD [removed] Add to Reading List Source URL: ontology.buffalo.edu Language: English - Date: 2012-04-25 15:43:49 Information science Semantic Web Technical communication Ontology Knowledge Informed consent Clinical research coordinator Consent Information Science Knowledge representation
497	SAMPLE CONSENT FORMS TEMPLATE C: STUDENT INVESTIGATOR AND ADULT SUBJECTS University of North Texas Institutional Review Board Informed Consent Form Add to Reading List Source URL: research.unt.edu Language: English - Date: 2014-08-22 16:22:45 Applied ethics Medicine Design of experiments Pharmacology Drug safety Institutional review board Informed consent Clinical research coordinator Clinical trial Clinical research Medical ethics Research
498	INDIANA UNIVERSITY EAST AUTHORIZATION FOR THE RELEASE OF HEALTH INFORMATION FOR RESEARCH Introduction: You have the right to decide who may review or use your Protected Health Information ("PHI"). The type of informati Add to Reading List Source URL: www.iue.edu Language: English - Date: 2009-03-10 14:52:47 Health Medicine Pharmaceutical industry Design of experiments Medical informatics Clinical research coordinator Food and Drug Administration Institutional review board Medical record Clinical research Pharmacology Research
499	Emerson Strategic Group, Inc. Confidential – For Internal IUSM Use & Reference Only Page < PAGE >1 Indiana University East v08/2008 Add to Reading List Source URL: www.iue.edu Language: English - Date: 2011-02-04 09:12:57 Design of experiments Pharmacology Ethics Scientific method Drug safety Institutional review board Clinical research coordinator Health Insurance Portability and Accountability Act Authorization Clinical research Pharmaceutical industry Research
500	Microsoft Word - Burris - EE[removed]doc Add to Reading List Source URL: www.law.northwestern.edu Language: English - Date: 2007-08-05 11:30:00 Ethics Institutional review board Office for Human Research Protections Clinical trial Human subject research Public Responsibility in Medicine and Research Adverse event Audit Clinical research coordinator Clinical research Research Science

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