Medical Director-IRB
Mercy · Mercy Virtual Care Center
What the posting says
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- Employment typeStated
- Part time
- Work arrangementStated
- Hybrid
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- PayNot mentioned
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Requirements, each with its sentence from the posting
These are the employer’s words. The index does not judge whether you meet them.
- Advanced degree in relevant scientific, medical, or legal disciplinerequired
Advanced degree in a relevant scientific, medical, or legal discipline.
from the posting - Understanding of human subjects research regulations and Common Rulerequired
Demonstrated deep understanding of human subjects research regulations, the Common Rule, and bioethics.
from the posting - Knowledge of bioethicsrequired
Demonstrated deep understanding of human subjects research regulations, the Common Rule, and bioethics.
from the posting - Interpersonal skillsrequired
Exceptionally strong interpersonal, conflict-resolution, and clear written communication skills
from the posting - Conflict resolutionrequired
Exceptionally strong interpersonal, conflict-resolution, and clear written communication skills
from the posting - Written communication skillsrequired
Exceptionally strong interpersonal, conflict-resolution, and clear written communication skills
from the posting
Read the full posting as the employer wrote it
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 Details:
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
- Meeting Leadership: Preside over convened full-board IRB meetings, manage protocol discussions, and facilitate consensus voting on complex ethical issues.
- Protocol Review: 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.
- Regulatory Compliance: 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.
- Committee Oversight: Mentor and train IRB members and administrative staff on evolving regulatory updates and ethical review standards.
- Researcher Liaison: Advise investigators on protocol design, consent form requirements, and human subject risk mitigation strategies.
- Corrective Action: Authorize the suspension or termination of research approvals when required to protect participant safety.
Qualifications
- Education: Advanced degree in a relevant scientific, medical, or legal discipline.
- Expertise: Demonstrated deep understanding of human subjects research regulations, the Common Rule, and bioethics.
- Skills: Exceptionally strong interpersonal, conflict-resolution, and clear written communication skills
Why Mercy?
From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.
Join a caring, collaborative team where your voice matters. At Mercy, you'll help shape the future of healthcare through innovation, technology, and compassion. As we grow, you'll grow with us.
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