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Trainee Irb Analyst Jobs (NOW HIRING)

Senior Regulatory Analyst - Yale IRB

$118K - $119K/yr

Position Focus The Senior Analyst, Human Research Protection Program (HRPP) supports the Yale HRPP ... trainees regarding human research standards and institutional requirements; 3. coordinate and ...

Research Data Analysts

Campus, IL · On-site

$21 - $24/hr

Contribute to the preparation and submission of grant applications, Institutional Review Board (IRB ... Research Data Analyst II: Requires a bachelor's (or equivalency) + 4 years or a master's (or ...

Research Data Analysts

Campus, IL · On-site

$21 - $24/hr

Contribute to the preparation and submission of grant applications, Institutional Review Board (IRB ... Research Data Analyst II: Requires a bachelor's (or equivalency) + 4 years or a master's (or ...

Research Data Analysts

Campus, IL · On-site

$21 - $24/hr

Contribute to the preparation and submission of grant applications, Institutional Review Board (IRB ... Research Data Analyst II: Requires a bachelor's (or equivalency) + 4 years or a master's (or ...

Research Associate

Camden, NJ · On-site

$23 - $37/hr

Assists the Principal Investigator and other members of the research team with preparation of IRB ... Proficiency in Adobe Photoshop and statistical analyses. Conduct basic and translational research ...

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How much do trainee irb analyst jobs pay per year?

As of Jun 11, 2026, the average yearly pay for trainee irb analyst in the United States is $92,170.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $116,500.00 per year, depending on experience, location, and employer.

What is the difference between Trainee Irb Analyst vs Junior Clinical Research Coordinator?

AspectTrainee Irb AnalystJunior Clinical Research Coordinator
Required CredentialsTypically a bachelor's degree in health sciences or related field; some certifications preferredBachelor's degree often required; certifications like CCRP are a plus
Work EnvironmentOffice-based, reviewing IRB submissions and compliance documentsClinical sites, coordinating study activities and participant management
Employer & Industry UsageResearch institutions, hospitals, biotech companiesPharmaceutical companies, research sites, hospitals

The Trainee Irb Analyst primarily focuses on reviewing and ensuring IRB compliance, working in an office setting. In contrast, a Junior Clinical Research Coordinator manages study logistics and participant interactions at clinical sites. Both roles require related educational backgrounds but differ in daily tasks and work environment.

What are some typical challenges a Trainee IRB Analyst might face during their initial months on the job?

As a Trainee IRB Analyst, one common challenge is quickly learning the complex federal regulations and ethical guidelines governing human subjects research. New analysts often spend significant time interpreting protocol submissions and ensuring compliance, which can be overwhelming at first due to the detail-oriented nature of the work. Additionally, adapting to the collaborative review process—working closely with senior analysts, board members, and researchers—requires strong communication skills and a willingness to ask questions. With training and mentorship, most trainees gain confidence and proficiency within a few months.

What are Trainee IRB Analysts?

Trainee IRB Analysts are entry-level professionals who assist Institutional Review Boards (IRBs) in reviewing research proposals to ensure they comply with ethical standards and federal regulations. They typically help with the initial review of submissions, communicate with researchers regarding required changes, and support more experienced analysts in the review process. This role is ideal for individuals interested in research ethics, regulatory affairs, or compliance within academic or healthcare settings.

What are the key skills and qualifications needed to thrive as a Trainee IRB Analyst, and why are they important?

To thrive as a Trainee IRB Analyst, you need a background in research ethics, regulatory compliance, and an understanding of human subjects protection, often supported by a bachelor’s degree in a related field. Familiarity with IRB management systems, federal regulations like the Common Rule, and certifications such as CITI training are typically required. Attention to detail, strong organizational skills, and effective communication help you excel when reviewing protocols and interacting with researchers. These skills are crucial to ensure ethical research oversight, regulatory adherence, and the safeguarding of participant rights and welfare.
More about Trainee Irb Analyst jobs
What cities are hiring for Trainee Irb Analyst jobs? Cities with the most Trainee 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 Trainee Irb Analyst jobs? States with the most job openings for Trainee Irb Analyst jobs include:
Infographic showing various Trainee Irb Analyst job openings in the United States as of June 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 81% Physical, 8% Hybrid, and 11% Remote job distribution, with an average salary of $92,170 per year, or $44.3 per hour.
Senior Regulatory Analyst - Yale IRB

Senior Regulatory Analyst - Yale IRB

Yale University

Remote

$118K - $119K/yr

Full-time

Posted 26 days ago


Yale University rating

8.7

Company rating: 8.7 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

40th of 535 rated colleges and universities


Job description

Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Discover your opportunities at Yale!
Position Focus
The Senior Analyst, Human Research Protection Program (HRPP) supports the Yale HRPP and University's research mission by providing guidance and support to the committees managed by the HRPP, including the Yale designated IRB (e.g., the Yale IRB or an external IRB authorized by the Yale Human Research Protection program (HRPP) to provide review of Yale research on behalf of Yale). In the performance of duties for this position, the Senior Analyst will: 1. apply relevant ethical principles, regulations, guidelines, policies, and other standards to ensure the ethical protection of human research participants, compliance, and the appropriate conduct of research; 2.serve as a resource to researchers, study personnel, employees, students, fellows, and trainees regarding human research standards and institutional requirements; 3. coordinate and facilitate the review of biomedical and behavioral research studies submitted for review and approval; 4. Demonstrate quality, productivity, efficiency, innovation, accountability, consensus building, teamwork, customer service, professionalism, inclusiveness, problem solving, and effective communications skills in all work performed by the HRPP office; and 5.Demonstrate ethics, integrity, organizational commitment, and alignment with the HRPP and Yale's missions and goals.
On Campus Schedule: Largely Remote
Required Skill and Abilities
1.Sophisticated knowledge of applicable legal, regulatory, and medical terminology and demonstrated expertise and ability to interpret, analyze, apply, and communicate (verbally and in writing) applicable ethical principles, standards, regulations, guidance, policies, and academic and industry trends that impact human research.
2.Demonstrated ability to effectively interact and collaborate with a broad spectrum of individuals including faculty, patients, participants, researchers, administrators, students, agency representatives, and other professional contacts.
3.Proven ability to process a large volume of complex work by prioritizing and organizing work and demonstrating flexibility and willingness to adjust priorities as necessary to meet conflicting demands.
4.Strong software application skills and demonstrated ability to learn new software packages; highly skilled in office productivity software (e.g., Word, PowerPoint, Excel, e-mail, Outlook, and Adobe, etc.)
5.Detail oriented with proven organizational skills, analytical/problem solving abilities, and sound professional judgment.
Preferred Education, Experience and Skills
1.A Master's level or other advanced degree in law, nursing, public health, or related field and five or more years Institutional Review Board, research administration, or other relevant research-related experience at a large academic institution, hospital/medical center, academic/independent IRB, non-profit/foundation, or an industry/corporate environment.
2.Professional certification (e.g., Research Compliance Certification, Certified IRB Professional, or other research-related certification).
Principal Responsibilities
1. Review submissions and work with the study teams to ensure that study materials are complete.
2. Communicate with investigators and assist with the preparation and editing of protocols, consent forms, and other study-related documents to ensure that research that is presented for review is consistent with University policies and meets the applicable ethical and regulatory standards for review and approval.
3. Ensure that necessary University, Yale-New Haven Hospital (YNHH), ancillary committee, and other required approvals and agreements are complete for a study submitted for IRB Review.
4. Determine the types of review required for research studies to ensure they are properly categorized and routed for review.
5. Ensure that investigators are qualified and meet applicable requirements to serve as a Principal Investigator for studies submitted for review.
6. Evaluate and analyze research studies to identify human subjects research issues and ensure that the submissions are ready for review.
7. Apply applicable ethical principles, standards, regulations, guidelines, and policies to the review of research studies, including the protocol, consent form, and other study-related documents.
8. Identify and resolve issues related to the approvability or ongoing approval of submissions prior to their review and escalate matters as necessary.
9. Route information and communicate study-related findings to the Principal Investigator or other designated individuals as appropriate throughout the review process and communicate and explain to the Principal Investigator any pre-approval, post-approval, or other required modifications related to a research study.
10. Attend committee meetings, participate in discussion, and prepare meeting minutes and other correspondence that reflect the committee's determinations as assigned.
11. Ensure that written information and committee determinations and determination letters are accurate and complete.
12. Assist with the review of compliance matters, reportable new information, assessments, inspections, and audits.
13. Assist with departmental projects, cross-departmental initiatives, and training and education.
14. Review, recommend, and revise applicable policies, standard operating procedures, work instructions, guidance, checklists, forms, and other documents to ensure compliance with applicable ethical principles, standards, regulations, guidelines, and policies.
15. Serve as a member or consultant on a University committee such as the Yale IRB or other committee as requested and exercise delegated IRB Chair signature authority to conduct expedited determinations on behalf of the IRB.
16. Other duties as assigned.
Required Education and Experience
Bachelor's degree in a related field and five or more years of research-related experience or an equivalent combination of education and experience.
Job Posting Date
04/16/2026
Job Category
Professional
Bargaining Unit
NON
Compensation Grade
Administration & Operations
Compensation Grade Profile
Manager; Program Leader (24)
Salary Range
$68,000.00 - $120,500.00
Time Type
Full time
Duration Type
Staff
Work Model
Remote
Background Check Requirements
All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks based on the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.
Health Requirements
Certain positions have associated health requirements based on specific job responsibilities. These may include vaccinations, tests, or examinations, as required by law, regulation, or university policy.
Posting Disclaimer
Salary offers are determined by a candidate's qualifications, experience, skills, and education in relation to the position requirements, along with the role's grade profile and current internal and external market conditions.
The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific duties and responsibilities of the position. Employees will be assigned specific job-related duties through their hiring department.
The University is committed to basing judgments concerning the admission, education, and employment of individuals upon their qualifications and abilities and seeks to attract to its faculty, staff, and student body qualified persons from a broad range of backgrounds and perspectives. In accordance with this policy and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual's sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran.
Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).
Note
Yale University is a tobacco-free campus.

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