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Chesterfield, Missouri
Source: Mercy careers · View original posting
From Mercy's posting. “We” and “our” refer to the employer.
Find your calling at Mercy!
As the Sisters of Mercy before us, we bring to life the healing ministry of Jesus through our compassionate care and exceptional service.
Position Summary
The Institutional Review Board (IRB) Chair provides administrative, ethical, and regulatory leadership for the institution’s human subjects protection program. The Chair oversees the review of all research involving human participants to ensure full compliance with federal regulations, state laws, and institutional policies. This role ensures the protection of the rights, safety, and welfare of human research subjects while facilitating ethical scientific advancement.
Core Responsibilities
Preside over convened full-board IRB meetings, manage protocol discussions, and facilitate consensus voting on complex ethical issues.
Conduct expedited and exempt reviews, evaluate protocol amendments, and handle standard adverse event or non-compliance reports. Oversee training of designated reviewers and ensure reviewer compliance with Mercy IRB SOPs and other applicable policies.
Interpret and apply federal regulations (e.g., DHHS 45 CFR 46, FDA 21 CFR 50/56), state statutes, and the ethical principles of the Belmont Report.
Mentor and train IRB members and administrative staff on evolving regulatory updates and ethical review standards.
Advise investigators on protocol design, consent form requirements, and human subject risk mitigation strategies.
Authorize the suspension or termination of research approvals when required to protect participant safety.
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