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Publish or Perish. Intensive Course on Research and Publishing in the field of Bioethics.

(Leuven, Belgium, 10 -12 October 2012)

The Centre for Biomedical Ethics and Law (of KU Leuven) is organising an intensive course on research and publishing in bioethics and medical humanities. Many researchers are struggling to get their work published. The objective of this course it to provide them and anyone interested in publishing in bioethics and the medical humanities with coherent information and support. The course offers all the necessary practical tools to get well-planned research work published.

The course will combine lectures with practical examples. There will be time for discussions. Participants will be invited to present their own research work in progress. The language of instruction will be English.

The course is of interest to participants from diverse professional backgrounds, such as nursing, medicine, philosophy and theology, health care administration, to PhD students undertaking courses of study in these areas and to more senior researchers. Anyone interested in publishing in bioethics and the medical humanities will benefit from this course. This intensive course is part of the Erasmus Mundus Master of Bioethics programme organised by a consortium of three European universities, namely the KU Leuven (Belgium), Radboud Universiteit Nijmegen (The Netherlands) and the Università degli Studi di Padova (Italy). Because of this combination, participants of the intensive course will join Master students from all over the world.

The course fee is € 650 if you register and pay as a participant before August 1st 2012, € 750 for registration and payment from August 1st 2012 onwards. This fee includes tuition and course materials, as well as refreshments, three lunches and a dinner. Detailed information on registration and payment can be found at our website www.masterbioethics.org under Intensive Courses.

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Bookmarked by Editorial Team on 25 May 2012
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ASSISTANT DIRECTOR FOR RESEARCH ETHICS (3 year contract): VACANCY NO. ORD 1/2012

UNIVERSITY OF BOTSWANA

OFFICE OF RESEARCH AND DEVELOPMENT

ASSISTANT DIRECTOR FOR RESEARCH ETHICS (3 year contract): VACANCY NO. ORD 1/2012:

Duties: The successful candidate will develop the structure and management of the current system of research ethics protocol and approval for the University of Botswana, through formulation of policies and strategies where necessary, and documenting guidelines for researchers on how to secure ethical approval for their research at UB in accordance with the Botswana Government research permit system. Another key duty will be to develop a formal accredited training programme for staff, students and other stakeholders on research ethics.

Requirements: (i) Minimum Masters Degree in Bioethics or other relevant field. A doctorate would be an added advantage. (ii) At least three years successful and effective experience in development and administration of research ethics policy, in a University or equivalent organization.

Competencies: Personal integrity that places incumbent above conflict of interest and unethical conduct, high level of discretion in handling confidential information, efficiency in handling committee tasks, strong organisational and administrative skills; self motivated individual who works independently.

Remuneration: The University offers competitive salary and benefits. For more information on the University visit our website at: www.ub.bw
Applicants are to address the stated qualifications and, provide other information to assist the University to determine their suitability for the position. They should also quote the vacancy number of the post applied for, provide Current CV’s (including telephone, telefax and e-mail) certified true copies of educational certificates and transcripts as well as three references (including one from the current employer). Complete documentation should be sent to:

The Centre Administrator, Office of Research and Development, Private Bag UB 00708, Gaborone. Telephone (267) 355 2900; Fax (267) 395 7573. Online application forms may be accessed from www.ub.bw under “jobs” section. Applicants should inform their referees to: (i) Quote the vacancy number and position applied for and (ii) submit their references directly to the above address, before the stipulated closing date. E-mail: research@mopipi.ub.bw.

Hand delivered applications should be submitted to Office No. 150, CCE Block 243/150)

CLOSING DATE: Open until filled

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Bookmarked by pndexas on 16 May 2012
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Ethics of clinical trials outsourcing and conduct in LMICs, with a focus on India.

Clinical trials in India continue to be in the news, unfortunately a fair bit being negative coverage. Over the last few years, there has been continuing outrage on the issue of rising outsourcing of clinical trials to India, with concerns about little benefit or relevance to the public health needs of the country. While this dust has not even settled, allegations of unethical conduct in clinical trials have again brought a focus on the need for regulatory reform and stringent ethical safeguards.

India, as an emerging economy needs to continue to promote a strong culture of research and development, including in the health sector. However, attention needs to be paid to ensuring that stringent quality checks are built in, and that investigators conduct research in an impeccable manner. Failure to do so will dent the credibility of the research enterprise, affecting not just investigators or institutions conducting research, but also those planning to do so.

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Bookmarked by Anant Bhan on 10 May 2012
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Research for Health and Innovation Organiser (RHInnO)

The MARC project - Mapping of research ethics review and trial regulatory capacity in Africa - launched an online review platform for Research Ethics Committees: the Research for Health and Innovation Organiser (RHInnO) platform. The platform was demonstrated at the Forum 2012 in Cape Town, South Africa. The purpose of the platform is to facilitate an efficient ethical review clearance of clinical research involving human subjects.

International standards require that protocols of clinical research are reviewed by an independent research ethic committee (REC). However, many RECs in Africa lack the tools to coordinate efficiently the submission and review of protocols and timely communication to researchers. They face an increasing amount of paperwork. Resources and knowledge exchange are also limited.

RHInnO Ethics was created by the Web4Development team at the COHRED group. It aims to speed up the review process by improving efficiency. The system provides research ethics committees with a secure, web-based solution for tracking research applications throughout the entire life-cycle of the research project. This will improve control of research activities by the RECs and will contribute to safer management of submitted materials and minimize delays in communication within RECs and with researchers. Moreover, RHInnO will enable the committees to share standardised research regulation documents e.g. standard operating procedures and research review guidelines.

RHInnO takes away the complex process of creating paper-based data collection using a simple web application. The system offers a secure platform that allows users to enter and manage information about research projects and proposals, including principal investigator, reviewers, funding source, attachments, descriptions, comments and supporting documents. All available data is encrypted. Different interfaces are available, providing users access to specific information. Users can access a list of recent actions and alerts (e.g. the system will alert when a project is not complete, or when a new project has been submitted or approved). In addition, the system sends reminders to different user profiles (i.e. administrators, reviewers, researchers) to respond to pending requests promptly.

About MARC
The MARC project is an initiative funded by the European and Developing Countries Clinical Trials Partnership (EDCTP), and implemented through collaboration between the Council on Health Research for Development (COHRED) in Geneva, Switzerland and the South African Research Ethics Training Initiative (SARETI) at the University of KwaZulu-Natal, South Africa.

The MARC project (Mapping of ethics review and trial regulatory capacity in Africa) aims to develop an interactive and continuously updated map of Africa’s health research ethics committees (RECs) and to provide a web-based platform to increase contact and communication between these committees. A secondary objective is to map medicines regulatory authorities (MRAs) and facilitate a better contact between these authorities and research ethics review committees.www.researchethicsweb.org

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Bookmarked by Boitumelo Mokgatla on 3 May 2012
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Case Studies in the Ethics of Mental Health Research

The Journal of Nervous and Mental Disease (Volume 200, Number 3, March 2012)
Edited by Joseph Millum, Clinical Center Department of Bioethics/Fogarty International Center, NIH

Open access. Available at: http://journals.lww.com/jonmd/toc/2012/03000

According to the World Health Organization there are over 450 million people with mental, neurological or behavioral problems worldwide.

This collection presents six case studies in the ethics of mental health research, written by scientific researchers and ethicists from around the world. We publish them together as a resource for teachers of research ethics and a contribution to several on-going ethical debates. Each consists of a description of a research study that was proposed or carried out, and an in-depth analysis of the ethics of the study. The case studies are all freely available on-line from the journal’s website.

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Bookmarked by Editorial Team on 18 Apr 2012
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