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Clinical research coordinator
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#	Item
481	Montana Working Group to Improve Access to Clinical Trials Consensus Agreement for Healthcare Coverage of Routine Patient Care Costs Associated with Oncology Clinical Trials DRAFT DEFINITIONS I. Add to Reading List Source URL: www.csi.mt.gov Language: English - Date: 2011-10-21 16:02:30 Pharmacology Clinical research Medical statistics Food and Drug Administration Pharmaceutical industry Clinical trial Investigational New Drug Clinical research coordinator Phases of clinical research Research Health Medicine
482	Chadron State College Institutional Review Board Request for Administratively-Reviewed Exempt Certification Submit one complete copy to IRB Administrative Chair – allow at least two weeks for review Research Project T Add to Reading List Source URL: www.csc.edu Language: English - Date: 2012-11-09 22:46:18 Medical ethics Research Research ethics Design of experiments Pharmacology Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Ethics Applied ethics
483	[removed][removed]Department Name) University of the Fraser Valley[removed]King Road Add to Reading List Source URL: www.ufv.ca Language: English - Date: 2014-10-06 06:09:34 Research Ethics Pharmaceutical industry Informed consent Research ethics Internet privacy Clinical research coordinator Clinical trial Applied ethics Medical ethics Clinical research
484	SAMPLE CONSENT FORMS TEMPLATE D: STUDENT INVESTIGATOR AND PARENT GUARDIAN CONSENT WITH MINOR ASSENT (AGES[removed]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 16:21:48 Applied ethics Design of experiments Pharmacology Medicine Drug safety Institutional review board Informed consent Clinical research coordinator Medical ethics Clinical research Research
485	Clinical Trial Research News From the Office of Clinical Research Volume 13, Issue 4 October 2011 Add to Reading List Source URL: www.sbrc.ca Language: English - Date: 2011-10-11 11:34:20 Medical statistics Health Science Pharmacology Design of experiments Clinical trial Adverse event Clinical research coordinator Clinical research Research Pharmaceutical industry
486	SAMPLE CONSENT FORMS TEMPLATE E: FACULTY/STAFF INVESTIGATOR - INFORMED CONSENT NOTICE AND ADULT SUBJECTS University of North Texas Institutional Review Board Informed Consent Notice Add to Reading List Source URL: research.unt.edu Language: English - Date: 2014-08-22 16:23:25 Research Applied ethics Research ethics Design of experiments Pharmacology Institutional review board Informed consent Human subject research Clinical research coordinator Clinical research Medical ethics Ethics
487	RESEARCH ETHICS SUBMISSION FORM Please complete ALL information. Forms with incomplete information will not be reviewed. Submissions MUST be typed in an easy-to-read font. Any questions related to this form should be di Add to Reading List Source URL: www.avdha.nshealth.ca Language: English - Date: 2014-01-27 13:49:17 Science Ethics Food and Drug Administration Medical ethics Pharmacology Clinical research coordinator Clinical trial Informed consent Internet privacy Clinical research Research Pharmaceutical industry
488	Clinical Trial Research News From the Office of Clinical Research Volume 9, Issue 6 To Contact Us: Add to Reading List Source URL: www.sbrc.ca Language: English - Date: 2011-09-07 18:51:32 Covariance and correlation Evaluation methods Research methods Scatter plot Linear regression Correlation and dependence Plot Clinical research coordinator Regression estimation Statistics Regression analysis Econometrics
489	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 16:27:23 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
490	RTF Document Add to Reading List Source URL: www.iue.edu Language: English - Date: 2010-04-28 09:57:00 Medical ethics Applied ethics Drug safety Design of experiments Pharmacology Institutional review board Informed consent Clinical research coordinator Investigational New Drug Clinical research Ethics Research

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