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Irb Analyst Jobs (NOW HIRING)

This position requires knowledge of IRB policies and procedures, and Federal Regulations for clinical trials. * The Regulatory Analyst must be able to assist on the following studies: Investigator ...

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Irb Analyst information

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$31K

$73.3K

$130K

How much do irb analyst jobs pay per year?

As of Aug 17, 2026, the average yearly pay for irb analyst in the United States is $73,261.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $87,000.00 per year, depending on experience, location, and employer.

What is an IRB analyst?

An IRB (Institutional Review Board) Analyst is responsible for reviewing research proposals to ensure they comply with ethical guidelines and regulatory requirements for human subjects' protection. They assess study protocols, verify informed consent procedures, and ensure adherence to federal and institutional policies. IRB Analysts collaborate with researchers to address compliance issues and provide guidance on ethical research practices. Their role is critical in safeguarding participants' rights and welfare while facilitating ethical research.

What are the key skills and qualifications needed to thrive as an IRB analyst?

To thrive as an IRB Analyst, you need a strong background in research ethics, regulatory compliance, and an understanding of human subjects research, often supported by a relevant bachelor's or master's degree. Familiarity with electronic protocol management systems, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are highly valued. Strong attention to detail, analytical thinking, and effective communication skills set outstanding IRB Analysts apart. These qualities are crucial to ensure thorough, ethical review of research protocols and strict adherence to regulatory standards, protecting the rights and welfare of research participants.

What are some common challenges faced by IRB analysts in their daily work?

IRB Analysts frequently navigate complex regulatory requirements while reviewing a diverse range of research protocols, which can present challenges in interpreting guidelines and ensuring full compliance. They must balance efficiency with thoroughness, often working under tight deadlines to support both researchers and institutional standards. Staying current with evolving ethical standards and federal regulations is essential, as is effectively communicating decisions to investigators who may have varying levels of experience. Despite these challenges, the IRB Analyst role is rewarding for those who value ethical oversight and enjoy collaborative, detail-oriented work.

What do you need to be an IRB analyst?

To become an IRB analyst, candidates typically need a bachelor's degree in a related field such as healthcare, research, or ethics, along with experience in research compliance or regulatory environments. Knowledge of federal regulations like the Common Rule and Good Clinical Practice (GCP) is essential, and certifications such as the Certified IRB Professional (CIP) can enhance qualifications. Strong attention to detail, analytical skills, and the ability to review research protocols are also important for the role.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements set by Institutional Review Boards. They evaluate study procedures, consent forms, and risk assessments, often using specialized software, to protect research participants and maintain compliance. IRB analysts typically have a background in research ethics, healthcare, or related fields and work closely with researchers and regulatory bodies.

What cities are hiring for Irb Analyst jobs?

Cities with the most Irb Analyst job openings:

What are the most commonly searched types of Irb Analyst jobs?

The most popular types of Irb Analyst jobs are:

What states have the most Irb Analyst jobs?

States with the most job openings for Irb Analyst jobs include:

Infographic showing various Irb Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution, with an average salary of $73,261 per year, or $35.2 per hour.

$135K/yr

Full-time

Posted 24 days ago


Job description

POSITION RESPONSIBILITIES
  • Provides leadership, guidance and management on all aspects of day-to-day operations, maintaining a culture of excellence, superior end-to-end service and rapid turnaround times.
  • Oversees OHRA review committees including IRB and ancillary commmittees within the department. 
  • Oversees compliance with ClinicalTrials.gov, including an understanding of intersecting regulations governing human subjects research.
  • Serves a key leader within the institution, proactively collaborating with Montefiore Einstein leadership on system-wide process improvement and compliance functions. 
  • Oversees IRB software system, including overarching process, functionality, and troubleshooting of issues. 
  • Ensures compliance with internal/external policies & requirements. Maintains current knowledge/expertise in federal, state, local & institutional policies, procedures & guidelines.
  • Partners with Executive Director and departmental leadership to pro-actively identify areas for quality improvement, including QI plans, assessment, and implementing training and improvement plans within the department.
  • Assists with OHRA policy and procedure development to inform best strategic approaches & enhance effectiveness.
  • Serves as a voting member of the IRB.
  • Serves as the direct supervisor of a team of IRB analysts and managers, including tracking performance and conducting annual performance evaluations. In consultation with the Executive Director, addresses staff conflict and individual performance issues.
  • Assists with evaluation of board composition and IRB member performance reviews on an ongoing basis.
  • Assists in identifying and tracking key IRB performance metrics and staff performance management. Ensures high quality reporting in alignment with institutional needs. 
  • In consultation with Executive Director, evaluates space and staffing needs.
  • Reviews IRB meeting minutes to ensure they are accurate and meet regulatory requirements.
  • Assists with onboarding/training new IRB members and providing ongoing education to current IRB members on various human research protections.
  • Assists with conducting training and education outreach for the research community.
  • In consultation with Executive Director, addresses issues of serious/continuing non-compliance and unanticipated problems involving risk to participants or others.
  • Serves as deputy to Executive Director, including acting in this capacity (with defined responsibilities) in his/her absence, attends meetings on behalf of the director, or serves as delegate on institutional committees, as needed.
  • Performs other related duties as assigned
QUALIFICATIONS
  • Bachelor's degree required.
  • Graduate degree in a relevant field (ethics, biology, philosophy, public heath, etc.) a plus.
  • 5-7+ years IRB administrative experience.
  • Equivalent combination of education and experience will be considered. 
  • CIP certification required within 6 months of hire.
  • Experience within an academic medical center strongly preferred. 
Minimum Salary RangeUSD $120,000.00/Yr.Maximum Salary RangeUSD $135,000.00/Yr.ABOUT US

This position presents an opportunity for an individual with a commitment to the ethical conduct of research and outstanding credentials to assist with the day-to-day operations of the human research protection program at Montefiore Einstein. 

Employment Type: OTHER