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Irb Regulatory Analyst Jobs (NOW HIRING)

The position provides regulatory support to William Paterson University's Institutional Review ... The IRB Analyst will coordinate and attend convened IRB meetings, maintain the Human Ethics ...

The position provides regulatory support to William Paterson University's Institutional Review ... The IRB Analyst will coordinate and attend convened IRB meetings, maintain the Human Ethics ...

This position requires knowledge of IRB policies and procedures, and Federal Regulations for clinical trials. The Regulatory Analyst 2 must be able to assist with the following studies: * Prepare and ...

This position requires knowledge of IRB policies and procedures, and Federal Regulations for clinical trials. The Regulatory Analyst 2 must be able to assist with the following studies: * Prepare and ...

Provides regulatory support and oversight for the Research Community and serves as a point of ... May serve as an official member of the Institutional Review Board (IRB) Committee and/or a ...

IRB Operations Manager

Princeton, NJ · On-site

$130K - $170K/yr

POSITION SUMMARY We are seeking an experienced IRB Operations Manager to join Vitalief as a ... research regulations and institutional policies. * Strong organizational, analytical, and ...

POSITION SUMMARY We are seeking an experienced IRB Operations Manager to join Vitalief as a ... research regulations and institutional policies. * Strong organizational, analytical, and ...

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Irb Regulatory Analyst information

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$39.5K

$85.8K

$130K

How much do irb regulatory analyst jobs pay per year?

As of Sep 10, 2026, the average yearly pay for irb regulatory analyst in the United States is $85,812.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What is an IRB Regulatory Analyst?

An IRB Regulatory Analyst is a professional responsible for ensuring that research studies comply with ethical standards and regulatory requirements set by Institutional Review Boards (IRBs). They review research protocols, consent forms, and related documentation to make sure that studies involving human subjects protect participants’ rights, safety, and privacy. IRB Regulatory Analysts also serve as a liaison between researchers and the IRB, assist with the submission process, and help interpret regulations such as those outlined in the Common Rule and FDA guidelines. Their work is vital for maintaining institutional compliance and upholding the integrity of research.

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

To thrive as an IRB Regulatory Analyst, you need a strong understanding of federal regulations, ethical principles in human subjects research, and a relevant bachelor’s degree, often in science or healthcare. Familiarity with electronic IRB management systems, regulatory databases, and applicable certifications such as CIP (Certified IRB Professional) is typically required. Excellent attention to detail, critical thinking, and effective communication skills set standout candidates apart in this analytical and compliance-driven role. These skills ensure the protection of research participants, institutional compliance, and the integrity of research processes.

How to become an IRB Regulatory Analyst?

To become an IRB Regulatory Analyst, candidates typically need a bachelor's degree in health sciences, biology, or a related field. Relevant experience in clinical research, knowledge of federal regulations such as 21 CFR and GCP, and strong attention to detail are important. Certification in research compliance or regulatory affairs can enhance job prospects.

What does an IRB Regulatory Analyst do?

An IRB Regulatory Analyst reviews and ensures compliance with institutional review board (IRB) policies and federal regulations for research involving human subjects. They prepare and submit documentation, monitor ongoing studies, and assist with protocol amendments to ensure ethical standards are maintained. Strong knowledge of regulatory guidelines and attention to detail are essential in this role.

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What states have the most Irb Regulatory Analyst jobs?

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Infographic showing various Irb Regulatory Analyst job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 2% As Needed, 86% Full Time, 9% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $85,812 per year, or $41.3 per hour.
William Paterson University
Real Estate • 1 - 5K employees

Part-time

Re-posted 18 days ago


Job description

Thank you for your interest in working at William Paterson University.

William Paterson University is a purpose-driven, proudly diverse community-designated as both a public Hispanic-Serving Institution and Minority-Serving Institution-committed to creating transformative academic, professional, and personal experiences as a powerhouse of progress. We foster a workplace that values growth, flexibility, and community, and we are recognized as a 2024 and 2025 Forbes' Best Employers by State, 2025 Great College to Work For, and honored with the NJBIZ Empowering Women Award.

Our 1,000 dedicated staff members enjoy competitive benefits, a four-day summer workweek, tuition support, and strong opportunities for internal promotion. Situated on a scenic suburban campus just 20 miles from New York City, WP offers a diverse, inclusive environment where your contributions fuel student success, economic and social mobility, and community engagement. Together, we empower our students through intentional, holistic support within flexible, innovative, and inclusive settings-preparing graduates to thrive professionally and personally, and to lead with a commitment to progress in New Jersey and beyond.

JOB SUMMARY

The IRB Analyst reports to the IRB Administrator within the Office of Sponsored Programs. The position provides regulatory support to William Paterson University's Institutional Review Board (IRB) and is primarily responsible for ensuring research protocols submitted to the IRB are reviewed and assessed in an efficient manner for completeness, accuracy and level of review according to applicable regulations and or institutional policy. The IRB Analyst will coordinate and attend convened IRB meetings, maintain the Human Ethics administration roles in the online platform Cayuse, support the IRB membership and serve as a resource to the research community. The IRB Analyst will provide guidance and assistance to research investigators and study coordinators with subject matter expertise on the protection of human subjects in the review and processing of research protocols.

For more information on the Office of Sponsored Programs at WP visit https://www.wpunj.edu/osp.

PRINCIPAL RESPONSIBILITIES

  • Provide administrative support to the software IRB review systems in place at WP (Cayuse) including study files (online and/or paper) that document protocol activity.
  • Independently performs critical regulatory support to WP IRB and manages daily operations of the IRB.
  • Provide guidance and consultation to IRB members and investigators regarding implementation of federal regulations, state law, and WP IRB policies and procedures.
  • Assist faculty, staff, students and study coordinators in the processing of proposals for the WP IRB.
  • Review and track new protocol submissions, amendments, adverse event reports, and progress reports.
  • Coordinate, schedule, and attend IRB meetings, including preparation of meeting agendas and accurate meeting minutes. Prepare and distribute review materials, agendas and minutes of IRB meetings to all IRB members.
  • Generate correspondence to investigators based on determinations made by an assigned reviewer or the Board, including notify investigators about impending study expiration.
  • Performs comprehensive pre-review analysis of submission documents for completeness and communicates all identified deficiencies to investigators.
  • Conduct local context review of studies that may include, but is not limited to, verifying training of the research team, reviewing consent forms for local context, reviewing financial disclosures for conflicts of interest, and escalating to the IRB administrator unanticipated problems or suspected non-compliance.
  • Maintain education and training to ensure current and up to date knowledge for all job-related aspects.
  • Assist the IRB Administrator in identifying areas for development and updating of IRB human subject protection procedures, guidelines, process improvement initiatives, and other special projects.
  • Other duties as appropriate to the position.

MINIMUM QUALIFICATIONS

  • Bachelor's degree in an appropriate field or an equivalent combination of education and experience.
  • Minimum 2 years of experience in IRB administration, clinical research, or regulatory compliance with human subjects.
  • Familiarity with MS Office programs and MS Windows operating system.

PREFERRED QUALIFICATIONS

  • Familiarity with Cayuse software platform (or similar grant management platform).
  • Familiarity with NJ law and regulations related to human research.
  • Certification as an IRB Professional (CIP).
  • Knowledge of the Common Rule (45 CFR 46) and other relevant requirements and guidelines related to the ethical study of human research subjects.

PERSONAL ATTRIBUTES AND SKILLS

  • Excellent written and oral communication skills.
  • Excellent time management skills.
  • Ability to work as an effective team member.
  • Ability to provide excellent customer service.
  • Ability to assist in establishing systems and procedures.

This description indicates the general nature and level of work performed by employees in the above job. It is not intended to be a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to the job.

Hourly Rate - $25/hour

Invitation to apply

Interested candidates will be prompted to complete an applicationand submit a cover letter and resume/CV.

Submission of all documents listed is required for consideration and all documents should be uploaded where prompted to upload your resume/cv.

General questions related to this application process, please contact talent@wpunj.edu

Salary Range:

Please see posting.

Total Rewards and Benefits:

Click here to view the total rewards of working at WP

William Paterson University is committed to protecting your privacy and will not sell your personal information.

EEO Statement

William Paterson University is dedicated to providing equal opportunities and equal access to all individuals regardless of race or ethnicity, sex/gender (including pregnancy), gender identity or expression, sexual orientation, age, disability, genetic information, marital status, civil union status, familial status, religion, national origin or citizenship, military service status, or any other category protected by law. William Paterson University does not discriminate on the basis of any category stated above or as prohibited by applicable law. Individuals from historically underrepresented backgrounds are encouraged to apply.

For more information, visit University Facts