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Irb Jobs in Emory, GA (NOW HIRING)

United-Digestive

Clinical Research Manager

Atlanta, GA · On-site

$85 - $125/hr

... IRB, sponsor, and organizational requirementsConduct quality reviews, implement SOPs and CAPAs, and maintain audit and inspection readinessRecruit, onboard, train, mentor, evaluate, and allocate ...

Denali Health

Clinical Research Coordinator (CRC)

Atlanta, GA · On-site

$23.25 - $31/hr

Institutional Review Board (IRB) requirements * Sponsor/CRO requirements * Site Standard Operating Procedures * Assist with maintaining complete and audit-ready regulatory and study files. * Ensure ...

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Irb information

What is an IRB?

An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects. The primary purpose of the IRB is to ensure that the rights, welfare, and privacy of participants are protected throughout the research process. IRBs review research proposals to ensure ethical standards are met and that risks to participants are minimized. They are required for most research conducted at universities, hospitals, and other organizations that receive federal funding.

What are the typical responsibilities of an IRB coordinator, and how do they interact with researchers and regulatory bodies?

An IRB (Institutional Review Board) coordinator is responsible for managing the review process of research protocols involving human subjects to ensure compliance with ethical standards and federal regulations. This role involves working closely with researchers to guide them through the submission process, reviewing applications for completeness, and facilitating communication between the IRB committee and research teams. Coordinators also serve as liaisons with regulatory bodies, maintain records, and help organize IRB meetings. Strong organizational, communication, and regulatory knowledge are essential, as coordinators often balance multiple projects and deadlines while ensuring research integrity and participant safety.

What are the key skills and qualifications needed to thrive as an IRB administrator, and why are they important?

To thrive as an IRB Administrator, you need expertise in research ethics, regulatory compliance, and human subject protection, usually supported by a relevant bachelor's or master's degree. Familiarity with IRB management software, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are typically required. Strong organizational skills, attention to detail, and effective communication are crucial for coordinating reviews and guiding researchers. These skills ensure ethical research practices, regulatory compliance, and the protection of research participants.

What is the difference between Irb vs Clinical Research Coordinator?

AspectIrbClinical Research Coordinator
Required CredentialsOften requires IRB training, ethics certificationRequires research experience, sometimes certifications
Work EnvironmentReview boards, research institutionsClinical sites, hospitals, research centers
Employer & Industry UsageUsed in research oversight, ethics reviewUsed in managing clinical trials, patient coordination
Common Search & Comparison IntentUnderstanding roles in research ethicsUnderstanding clinical trial management

IRBs (Institutional Review Boards) focus on ethical review and approval of research protocols, ensuring participant safety. Clinical Research Coordinators manage the day-to-day operations of clinical trials, including patient recruitment and data collection. While both roles are integral to clinical research, IRBs oversee ethical compliance, whereas Coordinators handle trial execution.

How to get an IRB job?

To get an IRB (Institutional Review Board) job, candidates typically need a background in research ethics, healthcare, or related fields, along with relevant experience. Certifications such as the CITI Program Human Subjects Research course are often required, and strong knowledge of federal regulations like 45 CFR 46 is beneficial. Positions may involve reviewing research protocols to ensure ethical standards are met and often require attention to detail and good communication skills.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements. They evaluate risks, consent processes, and study procedures, often working with institutional review boards to approve or modify research proposals. Strong attention to detail and knowledge of federal regulations are essential for this role.

What cities near Emory, GA are hiring for Irb jobs?

Cities near Emory, GA with the most Irb job openings:

Irb jobs near you
Infographic showing various Irb job openings in Emory, GA as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution.

Clinical Research Regulatory Coordinator - IRB Liaison

10 Children's Healthcare of Atlanta, Inc.

Atlanta, GA • On-site

$23.25 - $31/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Children's Healthcare of Atlanta is seeking a regulatory research professional to assist investigators in completing regulatory approvals for clinical trials and external/internal projects. You will liaison with the IRB and study sponsors, develop protocols, consents, and data collection tools, and maintain regulatory files across multiple trials. The role emphasizes accuracy, regulatory knowledge, and independent work to support ongoing research activities within the department.

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