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Clinical research coordinator
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#	Item
941	Research discoveries can improve people’s health. For more information call: Before you decide to become a research Add to Reading List Source URL: www.mcw.edu Language: English - Date: 2012-09-12 07:34:53 Applied ethics Office for Human Research Protections Human subject research Clinical research coordinator Institutional review board Clinical research Research Ethics
942	PDF Document Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:36:56 Clinical Trials Directive Declaration of Helsinki Clinical trial Informed consent Good Clinical Practice European Union Ethics Committee Clinical research coordinator Clinical research Research Science
943	PDF Document Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:36:38 Health Science Clinical Trials Directive Clinical trial Good Clinical Practice Medical research Clinical research coordinator Clinical research Research Pharmaceutical industry
944	PDF Document Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:36:11 Health Clinical trial Ethics Committee Randomized controlled trial Informed consent Patient participation Institutional review board Medical ethics Clinical research coordinator Clinical research Research Medicine
945	DOC Document Add to Reading List Source URL: www.inven2.com Language: English - Date: 2013-08-16 10:26:53 Scientific method Clinical trial Institutional review board Case report form Lost to follow-up Clinical research coordinator Clinical research Research Science
946	Maine Cancer Registry Application Checklist for Identifiable Data The following information must be submitted prior to the review of individual patient identifying information requests by the Cancer Registry Subcommittee Add to Reading List Source URL: www.maine.gov Language: English - Date: 2013-02-13 13:05:25 Medicine Medical statistics Health Clinical study design Scientific method Confidentiality Cancer Clinical research coordinator Institutional review board Design of experiments Science Clinical research
947	RESEARCH STUDY CPRS GUIDELINES Research Study Initiation Note – (RSIN)This is a template, which contains the study title, investigators’ and study coordinator’s names and contact numbers, potential side effects, a Add to Reading List Source URL: www.visn2.va.gov Language: English - Date: 2010-03-03 08:54:52 Pharmaceutical industry Healthcare Progress note Clinical research
948	Contents Module 1: Becoming an Investigator: Considerations................................................................... 8 Including Clinical Trials in Your Practice ............................................... Add to Reading List Source URL: training.cancer.gov Language: English - Date: 2009-11-02 14:38:44 Pharmacology Science Scientific method Design of experiments Clinical trial Clinical research coordinator Institutional review board Good Clinical Practice Cancer Trials Support Unit Clinical research Research Pharmaceutical industry
949	[removed]127000APPENDIX D 020000APPENDIX D Required Reports in Human Research per VHA ORO Handbook[removed], OHRP and local SOPs References to days mean business days. HUMAN RESEARCH (HB[removed], section 6, pg. 7-10) Add to Reading List Source URL: www.visn2.va.gov Language: English* - Date: 2014-04-21 10:17:44 Scientific method Office for Human Research Protections Human subject research Clinical research coordinator Institutional review board Clinical research Research Ethics
950	APPLICATION TO UNDERTAKE RESEARCH INVOLVING HUMAN SUBJECTS Add to Reading List Source URL: www.visn2.va.gov Language: English - Date: 2012-05-16 14:41:34 Clinical research Clinical research coordinator Pharmaceutical industry

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