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Clinical research coordinator
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51	Table of Contents - Stanford HRPP Policy Manual chapter 1................................................................................................................................................ 1 Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-08-12 17:42:03 Clinical research Medical ethics Design of experiments Research ethics Public Responsibility in Medicine and Research IRB Expanded access Human subject research Institutional review board Clinical research coordinator
52	DOC Document Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:57 Medical ethics Institutional review board Consent Right to withdraw Educational technology Protocol Clinical research coordinator
53	Title: FO 306 – Institutional Review Board Authorization Agreements for Review by External IRBs (IRB Reliance) Department: Sparrow Institutional Review Board 1.0 Policy: Add to Reading List Source URL: www.sparrow.org Language: English Clinical research ethics Medical ethics Design of experiments Clinical research Institutional review board Office for Human Research Protections Common Rule Grant IRB Human subject research Cooperative Human Tissue Network Clinical research coordinator
54	Consent Waiver) Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:49 Clinical research ethics Medical ethics Human subject research Clinical research Research ethics Office for Human Research Protections Informed consent Food and Drug Administration Institutional review board Clinical research coordinator
55	Stanford University IRB Guidance Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:51 Medical ethics Clinical research Human subject research Design of experiments Informed consent Clinical trial Consent Research participant Placebo-controlled study Food and Drug Administration Clinical research coordinator Institutional review board
56	DFG Project - KFO 243 Clinical Research Unit ELITE: Early Immunological Determinants of Late Transplant Outcome Coordinator: Prof. Edward K. Geissler, PhD – Head of Experimental Surgery Speaker: Prof. Dr. med. Hans J. Add to Reading List Source URL: www-kfo.uni-regensburg.de Language: English
57	Job Title: Clinical Research Project Coordinator Application Period: Present – Department: Delivra Inc. Add to Reading List Source URL: www.peibioalliance.com Language: English - Date: 2015-09-01 09:44:51
58	Research Coordinator THI Heart Valve Clinical Research (FT-RCOMPANY SUMMARY The mission of the Texas Heart® Institute is to reduce the devastating toll of cardiovascular disease through innovative programs in r Add to Reading List Source URL: www.texasheart.org Language: English - Date: 2015-10-01 15:35:27
59	See Does My Project Need IRB Review? If there is any question whether your project is human subject research you must submit this form to the IRB. Complete all sections then email to . Th Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-01-27 16:54:35 Clinical research Pharmaceutical industry Medical ethics Design of experiments Human subject research Clinical trial Office for Human Research Protections Food and Drug Administration Public Responsibility in Medicine and Research Clinical research coordinator
60	Research Coordinator Assistant THI Heart Valve Clinical Research (FT-RCOMPANY SUMMARY The mission of the Texas Heart® Institute is to reduce the devastating toll of cardiovascular disease through innovative pro Add to Reading List Source URL: www.texasheart.org Language: English - Date: 2015-10-01 15:27:27