IRB Specialist I - Research Compliance

1103 Team Member Services; United States; On-site; USD 33,000 - 61,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

PTO from day one

403(b) plan

Parental leave

Career development

Well-being resources

Mental health support

Pet benefits

Job summary

AdventHealth seeks an IRB professional to oversee regulatory reviews and protect human subjects in research. You will interpret complex CFR/IRB rules, coordinate with physicians and study teams, and ensure compliant documentation and submissions.

The role requires strong ethics, attention to detail, and the ability to manage multiple priorities in a fast-paced environment. Full-time daytime schedule in Orlando, FL, with comprehensive benefits.

Qualifications

• Knowledge of CFR, Common Rule (45CFR46) and FDA regulations impacting human subjects research.
• Excellent written and verbal communication, with strong grammar and tone.
• Ability to work independently and across departments while managing multiple priorities.

Responsibilities

• Applies regulations and approves submissions (new studies, modifications, renewals).
• Develops knowledge of state and federal laws governing protection of human subjects.
• Provides review decisions and assigns reviews to IRB members.
• Interacts with IRB manager, Chair, members, and researchers daily to facilitate reviews.
• Facilitates external IRB reviews when needed.
• Ensures information to the IRB from forms/documents is complete and consistent.
• Communicates policies and procedures in research administration.
• Interprets current regulations and trends affecting human subject research.
• Advises investigators and staff on compliance issues.
• Attends committee meetings as a resource on regulations.

Skills

Regulatory knowledge

Communication skills

Team collaboration

MS Office proficiency

Ethical conduct

Time management

Attention to detail

Education

Associate

Bachelor's (preferred)

Tools

IRB database software

MS Office Suite

Job description

AdventHealth seeks an IRB professional to oversee regulatory reviews and protect human subjects in research. You will interpret complex CFR/IRB rules, coordinate with physicians and study teams, and ensure compliant documentation and submissions.

The role requires strong ethics, attention to detail, and the ability to manage multiple priorities in a fast-paced environment. Full-time daytime schedule in Orlando, FL, with comprehensive benefits.