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You will provide secretariat support to the Centralised Institutional Review Board to ensure its effective and efficient operations. You will manage routine board functions, prepare management reports, facilitate department meetings, and coordinate projects to improve processes and regulatory compliance. You will review IRB applications for completeness, manage communications with Principal Investigators, and coordinate requests for clarification. You will also screen and process amendments, annual continuing reviews, protocol deviations, and serious adverse events. In addition, you will interpret and apply ethical principles for human biomedical research, serve as a resource for researchers on ethics matters, and develop and update forms, guidelines, policies, and educational materials.
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