Job Description & How to Apply Below
- Maintain policies amp practices that align with international norms for legal and ethical compliance and research governance
- Supervise and facilitate the operations of the IRB, meeting scheduling, agenda preparation, and minutes documentation
- Inspect and verify timely review of research protocols and informed consent documents, maintaining compliance with laws and regulations
- Facilitate coordination with IRB committee for initial reviews, continuing reviews, and adverse event reporting
- Mentor and coach the research office team on the research process and ensure that all projects are on the right track
- Handle the IRB approval and assurance approval with the Ministry of Public health
- Follow up with researchers on progress reports for IRB renewal or project closure completion
- Inspect and verify research projects to ensure they are reviewed and approved by the QPHI IRB Chair members taking into account its ethical soundness and methodology as required by law
- Adhere to established document control policies amp procedures and participate in their regular review in conformance with best practices and to ensure compliance with internal and regulatory policies
- Other reasonable tasks as assigned by supervisor
- Bachelor s degree in a relevant field with 6-8 years of relevant full-time work experience in compliance or regulatory affairs/ Human Research/ administration, 2 of which at a supervisory level
- Holds the Certified IRB Professional (CIP) certification.
- Knowledge of the Qatari legal system an advantage
- Excellent writing skills with the ability to draft and edit a variety of written reports and communications and to articulate ideas clearly and concisely;
Arabic proficiency is an advantage - Proficiency in MS Office applications
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