School of Arts and Social Sciences 28 April 2010.

Slides:



Advertisements
Similar presentations
The Role of the IRB An Institutional Review Board (IRB) is a review committee established to help protect the rights and welfare of human research subjects.
Advertisements

An informed consent process for people with learning disabilities and their carers Dr Anita Young Health Services Research Group The Robert Gordon University.
The School Research Ethics Committee Welsh School of Architecture.
An Introduction to the Ethics Review Procedure Lindsay Unwin: Research & Innovation Services, UREC Secretary.
Experiences of Patient and Public involvement in the Research Process Roma Maguire Senior Research Fellow Cancer Care Research Team School of Nursing and.
Marian University is sponsored by the Sisters of St. Francis, Oldenburg. Human Subjects Research and the Marian University Institutional Review Board (IRB)
University Research Ethics Committee Workshop on procedure and data protection issues 30th May 2008.
University of Sussex Research and Enterprise Research Governance, Integrity & Ethics: Key things you need to know in 5 minutes! Isla-Kate Morris, Research.
Good Clinical Research Practice Guidelines For Informed Consent Presented by Catherine May Acting Research Practice Development Officer The Office of Research.
Understanding Research Ethics Dr Meera Warrier Research Development Coordinator Academic Practice
Human Research and Ethics Dr Michèle de Courcy Chair, Faculty of Education HEAG University of Melbourne.
TODAY’S TOPIC: Ethics – deconstructing consent and participation with “vulnerable” populations.
PREPARING FOR REVALIDATION. Licences issued Revalidation pilots ongoing to test the whole process – completion March 2011 Responsible Officers – to be.
GCP compliance for GenISIS  This presentation is intended for clinical staff involved in recruiting patients to the GenISIS (Genetics of Influenza Susceptibility.
Responsible Sponsorship A case study Dr Birgit Whitman, Head of Research Governance.
Developing information for participants in your research – getting started This presentation contains some exercises to help you get started. You can do.
Research Ethics-Integrity-Governance. University Initiative:The Catalyst? ‘02 Good Research Practice Standards & Procedure to Investigate Potential Research.
8 Criteria for IRB Approval of Research 45 CFR (a)
The Research Project: ethical approval process
Research Ethics A guide to principles and procedures
Psychology Departmental Research Ethics Board (Psych-REB) October 2013 Dr. Carlin J. Miller, Chair.
Supporting you to understand research governance and ethics Emily Lamont Senior Research Manager NFER Claire Easton Senior Research Manager NFER
The Learning Agreement, Intellectual Property Rights and Project Approval Professor Dianne Ford Director of PhD Studies, Faculty of Medical Sciences.
Ofsted framework 2012 Feedback from inspections carried out under the new framework and implications for clerks and governing bodies Clerks briefings April.
Human Research Ethics and Obtaining Ethics Approval
Introducing Research Ethics: Policy and Procedure
The work of the Research Ethics Committee Dr Carol Chu.
“What’s Ethics Got To Do With It” Presentation to the Canberra Evaluation Forum Gary Kent Head Governance Australian Institute of Health and Welfare.
Psychology Departmental Research Ethics Board (Psych-REB) October, 2007 Dr. Pascual-Leone, Chair.
Cardiff and Vale UHB Bwrdd lechyd Prifysgol Caerdydd a’r Fro NHS R&D Overview How to avoid the common pitfalls? Thomas Fairman Research Liaison Manager.
Research Ethics & Compliance Dr Simon Barrett Manager, Research Ethics & Compliance Monash Research Office.
The Linguistics Department Institutional Review Board Committee Silvina Montrul, chair Fred Davidson Irene Koshik Ryan Shosted September 22, 2008.
Staff and Departmental Development Unit Ethics and Ethical Review Dr Alice Temple Research Ethics Senior Training & Development Officer, SDDU.
Humanities and Social Sciences Research Ethics Committee (HSSREC) April 2014.
APPRAISAL OF THE HEADTEACHER GOVERNORS’ BRIEFING.
Welcome New IRB Members! Today we will discuss: Your Role in the IRB: What to Know The IRB Review Process Resources Human Research Protections.
Quality Assurance Dr Christopher Stevens
Human Research Ethics: Issues and Procedures Dr. Constance Jones Chair, Committee for the Protection of Human Subjects.
WELCOME to the TULANE UNIVERSITY HUMAN RESEARCH PROTECTION OFFICE WORKSHOP for SOCIAL/BEHAVIORAL RESEARCH (March 2, 2010) Tulane University HRPO Uptown.
Standard Circular 57 The purpose of this circular is to clearly set out the responsibility of educational establishments and services in the matter of.
8 th November 2007 Research: ethics and research governance Rossana Dowsett Research and Regional Development Division [Pre Award Support] University of.
AssessPlanDo Review QuestionYesNo? Do I know what I want to evaluate and why? Consider drivers and audience Do I already know the answer to my evaluation.
Chapter 2: Ethical Issues in Program Evaluation. Institutional Review Boards (IRBs) Federal mandate for IRBs –Concern during 1970s about unethical research.
THE INSTITUTIONAL REVIEW BOARD. WHAT IS AN IRB? An IRB is committee set up by an institution to review, approve, and regulate research conducted under.
Research ethics.
The research ethics review process Hazel Abbott, Chair University Research Ethics Committee.
Informed Consent Presented by Marian Serge, RN. Goals Informed consent process and form Title 38 CFR , Common Rule required elements and additional.
Application for Ethics Approval for MSocScP(SCS) Research Projects Tianyuan Li, Chairperson of the PS Departmental Ethics Committee (May 2015)
Research Ethics Dr Nichola Seare Aston Health Research & Innovation Cluster.
Slide 1 Standard Operating Procedures. Slide 2 Goal To review the standard operating procedures Creating the informed consent document Obtaining informed.
SEBE Ethics Information Rod Gameson & Richard Hall.
Applying for ethical approval
REFLECT: Recovery Following Intensive Care Treatment
IRB BASICS Ethics and Human Subject Protections Summer 2016
University of Central Florida Office of Research & Commercialization
Enrolling in Clinical Trials
Welcome New IRB Members!
Research Ethics: a short guide for Staff 2017/18
Research Ethics: a short guide for PhD students 2017/18
Postgraduate Research Student Supervision
Research Ethics Matthew Billington
University of Central Florida Office of Research & Commercialization
© 2016 The McGraw-Hill Companies, Inc.
Strengthening our Commitment to Accountability to Beneficiaries
The Learning Agreement, Intellectual Property Rights and Project Approval Professor Dianne Ford Director of PhD Studies, Faculty of Medical Sciences.
Research Ethics and Integrity Officer
Strengthening our Commitment to Accountability to Beneficiaries
Strengthening our Commitment to Accountability to Beneficiaries
Dr. Sarah Quinton, UREC Chair,
Human Participants Research
Presentation transcript:

School of Arts and Social Sciences 28 April 2010

 9.00 – 9.30 School Ethics Framework, Ethics procedures  9.30 – 9.45 Data Protection

 9.45 –  Informed Consent  Mental Capacity Act  Vulnerable adults & children  Covert research  Human Tissue Act – Coffee Break – Subject Specific case studies & breakout

 Framework is supportive of staff activities, and not intended to prohibit activity  Processes are meant to ensure good practice and a climate of reflective practice  Ethics Framework will itself remain flexible and subject to updating as appropriate, and as our experience grows

 Intention is to ensure that initial scrutiny and “sign off” takes place within the subject area, where minimal risk is identified  Current system of Departmental Committee => School Committee reflects this

Receives and authorises all student related RE forms and authorises where possible Provides feedback from curriculum and programme developments to School/University procedures Receives and stores RE1/RE4 on an annual basis Provides administrative support to Ethics Activities where required Receives all staff related RE forms and authorises where possible Provides feedback from subjects and practice to School/University procedures Receives RE forms not agreed at Dept level for authorisation Organises Annual Report/Audit Establishes process and procedure across School Reports to School Research Committee and liaises with University Ethics Working Party School Ethics Committee Dept R&E Committee Dept DQCRED Office

 RE1 - Staff Ethics Checklist  All academic staff in the School should complete form RE1. The form should be updated when substantial changes have occurred and preferably on an annual basis. These forms should be forwarded the Senior Administrator of the RED Office for attention of the Research Sub-Committee and will be deposited in the School's research record store.

 RE2 - Staff Research Projects  All staff undertaking new research projects should complete form RE2. This should then be discussed and approved at Subject Level (for example, this could be done at Departmental Research and Enterprise meetings). If there are no starred answers, then the RE2 should be approved at Departmental level.  If the research involves recruitment via the NHS governance approval must be sought from the local NHS Trust R&D department and ethical approval from the Local NHS Research Ethics Committee.

 RE2 Cont.  If the research involves recruitment via Social Services the project must also be reviewed by the Local Authority's Social Care Ethics Committee. If the research project involves major ethical issues, or will involve a conflict of interest, then it must be reviewed by the School Ethics Committee prior to being sent for external approval. If there is a legitimate reason for not seeking written consent, then this should be explained on form RE2. It is recommended that researchers consult the guidance of appropriate professional associations in relation to informed consent, for example from the British Sociological Association.

 RE3 - Undergraduate/  Masters Student Checklist  The student and Principal Supervisor/Tutor should complete form RE3 at the first supervisory meeting. Students will need to be informed of the School’s ethics procedures in advance of the first supervisory meeting, especially as they will be expected to have read the relevant University documents. The process of ethical review will be managed at departmental level and overseen by research supervisors. Supervisors will undertake expedited review when the potential harm to participants and others affected by the research is minimal.

 RE3 cont.  Where research involves more than minimal risk full ethical review should be carried out at Departmental Board/Ethics Committee  Where there are any concerns following this process the Supervisor will refer the issue to the School's Ethics Committee for full ethical review and approval

 RE4 – Participant Consent Form  Research or consultancy projects that involve face-to-face interviews, focus groups, direct observation or similar methods of data collection, should normally be given an Information Sheet (or leaflet) and be asked to sign Participant Consent Form (Form RE4).  All RE4 forms must be deposited in the School's research record store which is maintained by the RED office. 

 RE5 – Research Information for Participants  Potential recruits to research must be given sufficient information to allow them to decide whether or not to take part. Consequently before they are asked to sign a consent form, participants should be provided with an Information Sheet. This should be written in simple, non-technical terms and be easily understood by a lay person.

 RE5 cont.  The Information Sheet should normally contain the following: study title; invitation paragraph; purpose of the study; reason for being chosen; explanation that their participation is voluntary; explanation of methods; possible benefits of taking part; results of the research; who is organising or funding the research; who is reviewing the study.

 RE6 – Departmental Ethics Report  This form should be used where the Departmental Committee is unable to give approval to a project – the form records the Committee’s concerns

 RE7 – Undergraduate/Masters Student Checklist  To be completed for all research undertaken (funded and unfunded) by staff, in the event of Audit.

 RE8 – School Ethics Committee Report  To be completed by the Chair of the School Ethics Committee only when unable to approve the project.

 RE9 –Approval for Module based activity  To be completed by the Module Tutor as part of the Module Approval process  Newly introduced process, currently being piloted in the School  Intended mainly for UG taught modules, usually containing externally facing group- work

RE9 cont. Activities are not classified as 'research' per se and are therefore governed by health and safety concerns rather than by ethics. They are activities designed to contribute to the taught element of the module - any data collected is not normally treated as real research data and is discarded once the session is completed.

 School Website  Framework Document  RE suite of forms  Quick Guide  University Website  Shared Drive

 Research and Enterprise Development (RED) Office  Debra Shannon, School Registrar, Secretary to School Ethics Committee, ext 3180

 Members of School Ethics Committee  Dr Alison Holland, Chair  Dr Alex Cowan, Dept of Humanities  Dr Robert McKenzie, Dept of Humanities  Dr Matt Smith, Dept of Social Sciences  Dr Paul Langley, Dept of Social Sciences  Dr Craig McLean, Dept of Social Sciences  Matt Hargrave, Dept of Arts  Dr Ysanne Holt, Dept of Arts  Dr Lesley Twomey, Dept of Languages  Ben McConville, Dept of Media  Dr Ian Inglis, Dept of Media