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 Job Information
Title

Senior/Manager (Human Subject Protection Program)

Role Pls see below
Category Healthcare Services - Nursing
Healthcare Services - Administration
Healthcare Services - Allied Health
Healthcare Services - LaboratoryServices
Location Singapore
Company Credit Management Consultancy (Asia) Pte Ltd ,  Vacancies [ -- ] (Posted on Monday December 17th,2007 10:10 PM)
Experience 2 to 5 Years
Educational Qualification Bachelor's Degree-Graduate Degree (BA, BSc, BCom)
Skills Leadership
Microsoft Office
Others
Salary --
Career Level Management (Manager/Director of Staff)
Job Type Permanent
Job Status Full Time
Open to Foreigner NO
 Job Description

Senior/Manager (Human Subject Protection Program)


Jobs

You will assist the Management to lead the Research and Development Office (RDO) in providing the highest level of administrative support services for the Healthcare Group Human Subject Protection Program (HSPP). You will be responsible for an effective, efficient and robust research ethics review and approval process in Healthcare Group. The HSPP is accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP) in US and aims to promote and ensure that high quality and ethical research is conducted in the Healthcare Institutions. You will ensure that rights, safety and well being of patients/volunteers participating in clinical research are protected by working closely with the Management, Institutions and Investigators to oversee and ensure that the research conducted in Healthcare Group institutions upholds the core ethical principles of respect for persons, beneficence and justice, and the research studies is in total compliant with all applicable regulatory requirement, and guidelines of AAHRPP. You will also oversee and manage the operation of the Admin Support for Ethics (ASE) arm of Healthcare Group Domain-Specific Review Boards (DSRBs) and Research Quality Assurance (RQA) Program. You will also assist in developing a system of continuous monitoring and audit of clinical trials studies and research projects within the cluster.

The Requirements

· Masters/Degree in Medicine/Nursing/Health Sciences/Pharmacy or equivalent.

· At least four years of relevant working experience

· Experience in research ethics, clinical trial and pharmaceutical regulatory is an added advantage

· Previous research experience is desirable, but not necessary.

· Computer literacy in word processing, spreadsheets and databases is essential

Only Singapore or SPRs need to apply.

To apply, please email full resume in MS Word format attached with recent photograph to info@cmc.com.sg stating your current salary, expected salary and availability date.

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