Clinical research coordinator

Results: 1108



#Item
11Medical research / Applied ethics / Medical ethics / Clinical research ethics / Research / Human subject research / Clinical research / Design of experiments / Institutional review board / Public Responsibility in Medicine and Research / Informed consent / Clinical research coordinator

American Public University System March 2016 Institutional Review Board

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Source URL: www.apus.edu

Language: English
12Medical research / Medical ethics / Research / Health care / Autonomy / Clinical research / Pharmaceutical industry / Clinical research coordinator / Public Responsibility in Medicine and Research / Health Insurance Portability and Accountability Act / Informed consent / Medical privacy

UNM IRB PROTOCOL TITLE: Text VERSION DATE: Text INVESTIGATOR/RESPONSIBLE Text FACULTY: STUDENT INVESTIGATOR: Text

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Source URL: cancer.unm-intranet.com

Language: English - Date: 2014-10-07 17:53:04
13Medical research / Clinical research ethics / Medicine / Health care / Clinical research / Pharmaceutical industry / Medical ethics / Design of experiments / Institutional review board / Adverse event / Office for Human Research Protections / Adverse effect

Unanticipated Problems FERCAP International Conference Dr. Brad Waite, CIP Coordinator, International IRB Fellowship Western Institutional Review Board (WIRB) November 24, 2008

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Source URL: www.fercap-sidcer.org

Language: English - Date: 2010-02-19 02:38:05
14Clinical research ethics / Ethics / Design of experiments / Medical research / Applied ethics / Nursing ethics / Drug safety / Institutional review board / Public Responsibility in Medicine and Research / Clinical research coordinator

Institutional Review Board Standard Operating Procedure . University of Missouri-Columbia

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Source URL: research.missouri.edu

Language: English - Date: 2016-02-04 12:02:13
15Medical research / Clinical research ethics / Medical ethics / Applied ethics / Research / Human subject research / Clinical research / Design of experiments / Institutional review board / Informed consent / Belmont Report / Clinical research coordinator

HRPP GUIDELINE 207 Researcher Responsibilities Issuing Office: Office of Research Administration Responsible Officer: Human Protections Administrator

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Source URL: www.irb.purdue.edu

Language: English - Date: 2014-10-22 15:36:56
16Medical research / Clinical research / Clinical trial / Audit / Medicare / Electronic health record / Clinical research associate / Clinical research coordinator

Clinical Trial Billing HOME STUDY TEST Earn 3.0 Continuing Education Credits This test expires on October 31, 2016 (original release date: )

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Source URL: www.acrpnet.org

Language: English - Date: 2015-09-18 10:54:37
17Medical research / Medical ethics / Applied ethics / Research / Clinical research ethics / Design of experiments / Clinical research / Human subject research / Institutional review board / BDSM / Clinical trial / Clinical research coordinator

Approval Date: monthname dd, yyyy For the Assent of decisionally impaired ADULTS (18 or older) who are unable to provide consent (i.e., adults for whom LAR provides consent) Instructional text is in red and should be r

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Source URL: researchcompliance.stanford.edu

Language: English - Date: 2016-04-12 01:21:57
18Medical research / Medical ethics / Applied ethics / Ethics / Clinical research ethics / Clinical research / Design of experiments / Institutional review board / Human subject research / Clinical research coordinator

Microsoft Word - SOP - Subject Compensation.doc

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Source URL: research.missouri.edu

Language: English - Date: 2015-07-01 12:53:56
19Medical research / Clinical research / Pharmaceutical industry / Health / Food and Drug Administration / United States Public Health Service / Case report form / Adverse event / Institutional review board / Clinical research coordinator

Protocol reviewed: Review completed by: Protocol #:       Title:       Name:       Date:      

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Source URL: humansubjects.stanford.edu

Language: English - Date: 2016-04-12 01:21:51
20Medical research / Clinical research / Pharmaceutical industry / Clinical trials / Medical ethics / Informed consent / Principal investigator / Clinical research coordinator

ANNEX 2 Form AFAPPLICATION FORM for RESUBMITTED PROTOCOL REVIEW Protocol Number (To be assigned by REBH member secretary): ... Protocol Title: ...

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Source URL: www.health.gov.bt

Language: English - Date: 2016-07-05 05:03:16
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