Director - Human Research Subjects Protection Program
Sidra Medicine · Doha
وصف الوظيفة
About the role
The Director of the Human Research Subjects Protection Program leads the institution’s efforts to safeguard participants in research. This senior position ensures compliance with national statutes, regulations, and ethical standards, acting as the primary liaison with the Ministry of Public Health and U.S. Office for Human Research Protections.
Key responsibilities
- Maintain institutional compliance with Ministry of Public Health (MOPH) and OHRP requirements.
- Collaborate with regulatory committee chairs, department heads, and senior administration to support ethical research conduct.
- Oversee and coordinate HRPP activities across all relevant offices and staff.
- Develop, revise, and implement policies and procedures aligned with best practices and evolving regulations.
- Manage and supervise staff providing administrative and regulatory support to the IRB.
- Ensure timely and thorough review of all IRB submissions.
- Administer Responsible Conduct of Research training and ensure completion of required training for investigators and staff.
- Conduct quality‑assurance monitoring, investigate non‑compliance, and implement corrective actions.
- Serve as the organization’s authority on compliance issues and maintain up‑to‑date knowledge of human research protection guidance.
Required profile
- Extensive experience in human research protection and regulatory compliance.
- In‑depth knowledge of MOPH, OHRP, and related ethical standards.
- Proven leadership and staff management capabilities.
- Strong policy development and implementation skills.
- Ability to coordinate training programs and ensure organization‑wide compliance.
- Excellent communication and liaison skills with regulatory bodies.
Required skills
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Sidra Medicine
Doha
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