IRB Chair & Human Subjects Oversight Leader

Mercy Health; Chesterfield (MO); On-site; USD 150,000 - 190,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision coverage

Paid time off

Tuition support

Retirement matching

Job summary

Mercy Health in Missouri seeks an experienced IRB Chair to provide administrative, ethical, and regulatory leadership for the institution's human subjects protection program. You will oversee review of research involving human participants to ensure compliance with federal, state, and institutional policies, safeguarding participant rights and welfare while enabling ethical scientific progress.

The role includes leading full-board meetings, overseeing protocol reviews and adverse event reports,

Qualifications

• Advanced degree in a relevant scientific, medical, or legal discipline.
• Strong understanding of human subjects research regulations and bioethics.
• Excellent interpersonal, conflict-resolution, and written communication abilities.

Responsibilities

• Preside over 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 adverse event or non-compliance reports; oversee reviewer training.
• Interpret and apply federal regulations (e.g., DHHS 45 CFR 46, FDA 21 CFR 50/56), state statutes, and Belmont Report principles.
• 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.

Skills

Interpersonal skills

Conflict resolution

Written communication

Leadership

Regulatory acumen

Education

Advanced degree in a relevant field

Job description

Mercy Health in Missouri seeks an experienced IRB Chair to provide administrative, ethical, and regulatory leadership for the institution's human subjects protection program. You will oversee review of research involving human participants to ensure compliance with federal, state, and institutional policies, safeguarding participant rights and welfare while enabling ethical scientific progress.

The role includes leading full-board meetings, overseeing protocol reviews and adverse event reports,