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Irb Jobs in Boston, MA (NOW HIRING)

Clinical Research Manager

Boston, MA · On-site

$74K - $111K/yr

Serve as primary regulatory lead for the Tufts single IRB of record: prepare and maintain submissions, modifications, continuing reviews, reportable new information, consent revisions, reliance ...

Clinical Research Associate

Boston, MA · On-site +1

$20.16 - $29.01/hr

This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors, and federal regulatory agencies. The CRRCI will be trained on the institutional and ...

Clinical Research Associate

Boston, MA · Remote

$20.16 - $29.01/hr

This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors, and federal regulatory agencies. The CRRCI will be trained on the institutional and ...

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Irb information

See Boston, MA salary details

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How much do irb jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for irb in Boston, MA is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $25.73 and $53.52 per hour, depending on experience, location, and employer.

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 are the most commonly searched types of Irb jobs in Boston, MA?

The most popular types of Irb jobs in Boston, MA are:

What cities near Boston, MA are hiring for Irb jobs?

Cities near Boston, MA with the most Irb job openings:

Infographic showing various Irb job openings in Boston, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 81% In-person, 5% Hybrid, and 14% Remote job distribution, with an average salary of $85,556 per year, or $41.1 per hour.

IRB Vice Chair, Mass General Brigham - Remote Opportunity

Mass General Brigham

Somerville, MA • On-site, Remote

Full-time

Re-posted 11 days ago


Brigham and Women's Hospital rating

8.1

Company rating: 8.1 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

117th of 1,064 rated hospitals


Job description

Site: Mass General Brigham Incorporated
Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.
Job Summary
The Mass General Brigham (MGB) Institutional Review Board (IRB) Vice Chair is responsible for chairing convened IRB meetings on a regular basis and conducting expedited reviews as needed in compliance with federal, state, and local laws and regulations, MGB Policies and Procedures, and the ethical principles described in the Belmont Report. The Vice Chair leads meetings in an organized and collaborative manner engaging and respecting the perspectives of both the scientists and community board members. This position will lead the weekly Other Events Committee and conduct reviews of Other Events involving reportable new information submitted to the IRB. Depending on their contributed FTE, this position may also regularly conduct expedited reviews as designated by the IRB Chair. This position involves regular interaction with Principal Investigators and research team members to discuss their IRB applications and regular meetings with the IRB and HRA leadership to contribute to the development of policies and ethical approaches to the protection of human subject research.
Qualifications
RESPONSIBILITIES:
Convened Meeting Activities
1. Chair and act as a voting member of convened IRB meetings during which the IRB conducts: (i) initial and continuing review of research activities involving human subjects; (ii) review of proposed changes in approved research during the period of approval; (iii) review of unanticipated problems involving risks to subjects or others, including adverse events that are serious, unexpected and related to the research.
2. Ensure research reviewed at each convened meeting is assessed based on the federal regulatory "Criteria for Approval" and complies with all applicable federal, state and local regulations as well as institutional policies, procedures and guidelines.
3. Support and participate in IRB initiatives on diversity, equity and inclusion (DEI) with respect to the IRB membership, the approach to review of research, as well as the conduct of human subject research and translation into improved health care in our community.
4. Review and approve reviewer assignments for convened IRB meetings.
5. Guard the independence of the IRB decision process with respect to inappropriate outside influence or conflict of interest.
6. Participate as a voting member of the IRB charged with reviewing reports of possible serious or continuing noncompliance and making determinations regarding corrective and preventative action plans.
7. Act as a primary or secondary reviewer as needed for protocol items on the agenda of convened meetings.
8. Review and approve meeting minutes and PI correspondence of IRB determinations to include attendance at meetings; actions taken by the IRB; the vote on these actions, including: (1) the number of members voting for, against, and abstaining; (2) the basis for requiring changes in or disapproving the research; (3) a summary of controverted issues and their resolution; and (4) findings and determinations required by regulation.

9. Review changes made by the PI subsequent to a convened meeting as needed in order to secure approval.
10. Participate in ongoing education activities during and outside of IRB meetings and in orienting new members to IRB review policies and procedures.
11. Provide guidance to members on regulatory issues and institutional policies and procedures.

Other Events Committee
1. Prior to the weekly meeting, the IRB Chair (or designee) sends out an agenda for the meeting including brief descriptions and assessments of the OEs to be reviewed that week.
2. At the weekly meetings, the IRB Chair (or designee) gives a brief presentation on OEs in which an IRB action is yet to be determined.
3. The IRB Chair (or designee) informs Investigators in advance about regulatory requirements to report to federal agencies and institutional officials any event that meets the definition of UPIRTSO, as well as serious and/or continuing noncompliance.
4. If the noncompliance is determined not to be serious and/or continuing and the proposed corrective action plan is appropriate, the IRB Chair (or designee) documents review in the Insight expedited review checklist.
5. The IRB Chair (or designee) is responsible for note-taking during the OEC meeting and documenting the Committee's review determination and recommendations for IRB routing.

Expedited Review Activities
1. Work independently to review research activity submitted to the MGB IRB to

a. determine research is not human subjects research or a clinical investigation subject to IRB review;
b. determine if research meets exemption criteria
c. approve non-exempt minimal risk research using the expedited review procedure
d. approve minor changes in approved research
e. conduct continuing review of approved minimal risk research
f. review other events.
2. Review human research protocol submissions according to standard operating procedures to ensure that human subject research overseen by the MGB IRB complies with all applicable federal, state and local regulations as well as institutional policies and procedures and guidelines.
3. Compose correspondence to investigators articulating modifications required in the research to secure IRB approval and any questions, concerns, or clarifications that need to be addressed before IRB approval can be considered.
4. Identify requirement(s) for review by the ancillary committees, or communication or coordination with other departments, groups, or individuals within the institution that share responsibility for human subject protection.
5. Work with the research community in a collaborative manner to provide guidance and consultation to investigators and clinical research personnel about the MGB IRB policies and procedures and changes needed to secure IRB approval of submitted protocols.
6. Participate in meetings of designated Expedited Reviewers as needed.
7. Adhere to turnaround times for review and processing activities; identify opportunities for improvement; participate in process improvement activities; implement requested changes.
8. Other duties as assigned.

General Activities
1. Stay current on federal, state, local laws and regulations governing human subject research and attend conferences, workshops, seminars, or lectures that pertain to human subject protection.
2. Participate in periodic evaluations related to service on the IRB and evaluation of the IRB Chairs and HRO meeting staff.
3. If selected, participate in interviews with teams from the Association for the Accreditation of Human Research Protection Programs during on-site accreditation reviews which occur every 5 years.

Additional Job Details (if applicable)
QUALIFICATIONS:
  • Medical Doctor (MD) and 2 years of relevant experience.
  • Extensive knowledge of federal, state, and local laws and regulations governing human subjects research.
  • Certified IRB Professional (CIP) certification desirable.

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
1. Ability to conduct meetings in an effective and efficient manner
2. Excellent oral and written communication skills
3. Excellent organizational skills with ability to prioritize work and adhere to timelines
4. Ability to assess institutional and federal criteria, apply to a variety of situations, and make decisions based on specified criteria
5. Excellent interpersonal skills to effectively and professionally communicate and collaborate with researchers and staff at all levels of the organization and both scientific/medical and non-scientific/medical persons.
6. Ability to problem solve and successfully negotiate and collaborate with others of different skill sets, backgrounds and levels within and external to the organization
7. Self-motivated, independent and possesses the ability to learn quickly

Please note, this position can be a 0.75 - 1.0 FTE.
Remote Type
Remote
Work Location
399 Revolution Drive
Scheduled Weekly Hours
40
Employee Type
Regular
Work Shift
Day (United States of America)
Pay Range
$98,841.60 - $161,262.40/Annual
Grade
9
At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.
EEO Statement:
0100 Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.
Mass General Brigham Competency Framework
At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.

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