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Clinical research coordinator
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31	Rice University Consent Form for Participation in Research: Interview Study Title: Evaluating GitHub as a Platform of Knowledge Add to Reading List Source URL: digitalscholarship.files.wordpress.com Language: English - Date: 2016-05-11 19:03:06 Medical ethics Clinical research Autonomy Consent Tort law Interview Clinical research coordinator Privacy for research participants
32	Top of Form Education Department IRB Application: Cover Page Applicants are responsible for reading the Belmont Report and the Education Department Thesis manual prior to completing this application. Print and complete t Add to Reading List Source URL: wagner.edu Language: English - Date: 2014-08-19 14:13:03 Clinical research ethics Medical ethics Human subject research Clinical trials Experimental psychology Public Responsibility in Medicine and Research Informed consent Debriefing Clinical research coordinator Ethical research in social science
33	Version Date: March 2015 © Horizon Health Network – Ethics Services Internal Working Document Page 1 of 2 Add to Reading List Source URL: en.horizonnb.ca Language: English - Date: 2015-10-08 09:02:01 Clinical research Pharmaceutical industry Human subject research Medical ethics Informed consent Public Responsibility in Medicine and Research Constitutional amendment Clinical research coordinator Treaty
34	Job Title: Clinical Research Coordinator Position Type : Permanent, Full Time Job Description: Responsible for the implementation and coordination of clinical research studies and clinical trials. Duties: Key Duties: Add to Reading List Source URL: www.medicalresearchsouth.com Language: English - Date: 2016-02-29 18:02:56 Clinical research Pharmaceutical industry Clinical research coordinator Clinical trial Case report form Clinical Medicine Patient recruitment Monitoring in clinical trials
35	https://webirb.research.ucla.edu/WEBIRB/Doc/0/CE8URQKMVJT451LI624S35H462/fromString.html Add to Reading List Source URL: www.heri.ucla.edu Language: English - Date: 2016-01-14 19:15:55 Clinical research ethics Human subject research Medical ethics Design of experiments Institutional review board Regulatory compliance Informed consent IRB Higher Education Research Institute Clinical research coordinator
36	ANNEX 1 AF/01-007b/04 Contents of a Submitted Package Protocol Number:……………….. Initial Review Submitted Package Protocol Summary Sheet or Memorandum Application Form for Initial Add to Reading List Source URL: www.health.gov.bt Language: English - Date: 2016-06-29 07:05:29 Clinical research Pharmaceutical industry Clinical trials Design of experiments Medical ethics Informed consent Case report form Protocol Treaty Clinical research coordinator
37	ACRP_CR_Dec2015_HS_Section.pdf Add to Reading List Source URL: www.acrpnet.org Language: English - Date: 2015-11-23 12:15:03 Clinical research Pharmaceutical industry Clinical research associate Good clinical practice Clinical trial Clinical research coordinator Health informatics Case report form Clinical Monitoring in clinical trials Clinical trial portal
38	Microsoft Word - SOP - Reporting Requirements.doc Add to Reading List Source URL: research.missouri.edu Language: English Clinical research ethics Institutional review board Office for Human Research Protections Grant IRB Protocol Common Rule Clinical research coordinator Public Responsibility in Medicine and Research
39	FIERC Form 2.4 Informed Consent Evaluation Form Food and Nutrition Research Institute Ethics Review Committee Add to Reading List Source URL: www.fnri.dost.gov.ph Language: English - Date: 2016-03-04 07:48:20 Medical ethics Clinical research ethics Clinical research Human subject research Autonomy Informed consent Public Responsibility in Medicine and Research Consent Clinical research coordinator
40	DOC Document Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:57 Medical ethics Informed consent Health Insurance Portability and Accountability Act Institutional review board Consent Privacy Right to withdraw Human subject research Medical privacy Clinical research coordinator Privacy for research participants

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