We are devoted to nurturing a vibrant, inclusive community where every member - student, faculty ... Essential Functions * Directs the administration of the Institutional Review Board (IRB ...
We are devoted to nurturing a vibrant, inclusive community where every member - student, faculty ... Essential Functions * Directs the administration of the Institutional Review Board (IRB ...
IRB Submissions: Prepare, submit, and track initial protocols, amendments, continuing reviews, and ... Board Professional (CIP). * Technology: Proficiency with data management platforms for the ...
IRB Submissions: Prepare, submit, and track initial protocols, amendments, continuing reviews, and ... Board Professional (CIP). * Technology: Proficiency with data management platforms for the ...
IRB Submissions: Prepare, submit, and track initial protocols, amendments, continuing reviews, and ... Board Professional (CIP). * Technology: Proficiency with data management platforms for the ...
IRB Submissions: Prepare, submit, and track initial protocols, amendments, continuing reviews, and ... Board Professional (CIP). * Technology: Proficiency with data management platforms for the ...
Regulatory Specialist
Pittsburgh, PA · On-site
You will also serve as a resource to staff and member institutions. You would have a direct impact ... boards. * Researching regulatory issues pertaining to clinical trial protocols, consent forms ...
Regulatory Specialist
Pittsburgh, PA · On-site
You will also serve as a resource to staff and member institutions. You would have a direct impact ... boards. * Researching regulatory issues pertaining to clinical trial protocols, consent forms ...
... Review Board (IRB) members and staff, and other HRPP staff on human research protection and ... Serves as site inspection or assist visit team member for other HRPP staff members, as needed.
... Review Board (IRB) members and staff, and other HRPP staff on human research protection and ... Serves as site inspection or assist visit team member for other HRPP staff members, as needed.
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
... Review Board (IRB) members and staff, and other HRPP staff on human research protection and ... Serves as site inspection or assist visit team member for other HRPP staff members, as needed.
Human Research Protection Specialist, DONHRPP, Falls Church, Virginia
Falls Church, VA · On-site
$58K - $93K/yr
... Review Board (IRB) members and staff, and other HRPP staff on human research protection and ... Serves as site inspection or assist visit team member for other HRPP staff members, as needed.
This position will be a member of a multi-disciplinary team with the goal of providing ... Interdisciplinary Review Board (IRB) and monthly clinic meeting. * Assist in implementing quality ...
This position will be a member of a multi-disciplinary team with the goal of providing ... Interdisciplinary Review Board (IRB) and monthly clinic meeting. * Assist in implementing quality ...
Board Certified - Family Medicine or Internal Medicine Physician
Bayfield, WI · On-site
$130 - $160/hr
This position will be a member of a multi-disciplinary team with the goal of providing ... Interdisciplinary Review Board (IRB) and monthly clinic meeting. Assist in implementing quality ...
Board Certified - Family Medicine or Internal Medicine Physician
Bayfield, WI · On-site
$130 - $160/hr
This position will be a member of a multi-disciplinary team with the goal of providing ... Interdisciplinary Review Board (IRB) and monthly clinic meeting. Assist in implementing quality ...
... Boards (IRBs), and serves as a subject matter expert on human research protections. Job Duties ... Conducts compliance review of IRB minutes and protocol submissions to monitor compliance with ...
... Boards (IRBs), and serves as a subject matter expert on human research protections. Job Duties ... Conducts compliance review of IRB minutes and protocol submissions to monitor compliance with ...
Research Operations Coord
Augusta, GA · On-site
... member is responsible for demonstrating and upholding these standards ... More details on the USG Statement of Core Values and Code of Conduct are available in USG Board ...
Research Operations Coord
Augusta, GA · On-site
... member is responsible for demonstrating and upholding these standards ... More details on the USG Statement of Core Values and Code of Conduct are available in USG Board ...
Human Research Protection Program Analyst
Falls Church, VA · On-site
$90 - $130/hr
... Boards (IRBs), and serves as a subject matter expert on human research protections. Job Duties ... Conducts compliance review of IRB minutes and protocol submissions to monitor compliance with ...
Human Research Protection Program Analyst
Falls Church, VA · On-site
$90 - $130/hr
... Boards (IRBs), and serves as a subject matter expert on human research protections. Job Duties ... Conducts compliance review of IRB minutes and protocol submissions to monitor compliance with ...
The faculty member will also participate in scholarly activity and contribute to departmental ... Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access. Engage in ...
The faculty member will also participate in scholarly activity and contribute to departmental ... Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access. Engage in ...
The faculty member will also participate in scholarly activity and contribute to departmental ... Research/Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access.
The faculty member will also participate in scholarly activity and contribute to departmental ... Research/Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access.
The faculty member will also participate in scholarly activity and contribute to departmental ... Research/Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access.
The faculty member will also participate in scholarly activity and contribute to departmental ... Research/Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access.
The faculty member will also participate in scholarly activity and contribute to departmental ... Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access. Engage in ...
The faculty member will also participate in scholarly activity and contribute to departmental ... Scholarship - 10% Complete CITI training, IRB training and obtaining IRB online access. Engage in ...
Administer policies and procedures according to protocol, Institutional Review Board (IRB), grant ... Most importantly, it is each staff member's responsibility to project and maintain a positive ...
Administer policies and procedures according to protocol, Institutional Review Board (IRB), grant ... Most importantly, it is each staff member's responsibility to project and maintain a positive ...
Administer policies and procedures according to protocol, Institutional Review Board (IRB), grant ... Most importantly, it is each staff member's responsibility to project and maintain a positive ...
Administer policies and procedures according to protocol, Institutional Review Board (IRB), grant ... Most importantly, it is each staff member's responsibility to project and maintain a positive ...
... member is responsible for demonstrating and upholding these standards ... More details on the USG Statement of Core Values and Code of Conduct are available in USG Board ...
... member is responsible for demonstrating and upholding these standards ... More details on the USG Statement of Core Values and Code of Conduct are available in USG Board ...
Specialist, Clinical Trials
San Diego, CA · On-site
Manages essential document collection and Institutional Review Board (IRB) and Ethics Committee ... Serves as a team member for of assigned clinical studies * Prepares data / information for ...
Specialist, Clinical Trials
San Diego, CA · On-site
Manages essential document collection and Institutional Review Board (IRB) and Ethics Committee ... Serves as a team member for of assigned clinical studies * Prepares data / information for ...
Specialist, Clinical Trials
San Diego, CA · On-site
$90 - $123/hr
Manages essential document collection and Institutional Review Board (IRB) and Ethics Committee ... Serves as a team member for of assigned clinical studies * Prepares data / information for ...
Specialist, Clinical Trials
San Diego, CA · On-site
$90 - $123/hr
Manages essential document collection and Institutional Review Board (IRB) and Ethics Committee ... Serves as a team member for of assigned clinical studies * Prepares data / information for ...
Irb Board Member information
See salary details
$62K - $92.7K
6% of jobs
$92.7K - $123.5K
0% of jobs
$123.5K - $154.2K
0% of jobs
$154.2K - $184.9K
0% of jobs
$184.9K - $215.6K
4% of jobs
$215.6K - $246.4K
2% of jobs
$246.4K - $277.1K
1% of jobs
$307.8K is the 25th percentile. Wages below this are outliers.
$277.1K - $307.8K
11% of jobs
$307.8K - $338.5K
22% of jobs
The median wage is $342K / yr.
$338.5K - $369.3K
28% of jobs
$369.3K - $400K
25% of jobs
$62K
$330.1K
$400K
How much do irb board member jobs pay per year?
What is an IRB board member?
An IRB (Institutional Review Board) Board Member is responsible for reviewing research studies involving human subjects to ensure ethical standards and regulatory compliance. They evaluate study protocols, informed consent documents, and potential risks to participants. IRB members come from diverse backgrounds, including science, ethics, and community representation, to provide comprehensive oversight. Their role is critical in protecting participants' rights, safety, and well-being while supporting valuable research.
What are the typical responsibilities of an IRB board member during a protocol review?
As an IRB Board Member, your main responsibility is to carefully review research proposals involving human subjects to ensure that ethical standards and regulatory requirements are met. You will assess risks and benefits, evaluate the informed consent process, and discuss proposed studies in meetings with other board members, who may come from various scientific and non-scientific backgrounds. The role often involves reading detailed protocols, providing constructive feedback, and making decisions or recommendations about study approval, modifications, or disapprovals. This collaborative process helps ensure that research participants are protected and that studies are conducted according to governing guidelines. Serving as an IRB Board Member offers valuable experience in research oversight and can enhance your expertise in ethical decision-making.
What are the key skills and qualifications needed to thrive as an IRB board member?
To thrive as an IRB Board Member, you need a thorough understanding of research ethics, regulatory compliance, and principles of human subjects protection, often supported by advanced degrees in medicine, law, science, or ethics. Familiarity with federal regulations such as the Common Rule, use of electronic protocol management systems, and completion of IRB-specific training or certification (e.g., CITI Program) are typically required. Strong analytical skills, attention to detail, impartiality, and effective communication are vital soft skills for reviewing complex protocols and collaborating with diverse committee members. These qualifications and personal traits are crucial to safeguarding participants’ rights and welfare while enabling ethical research progress.
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Full-time
Posted 4 days ago
University Of Mississippi rating
7.9
Based on 17 frontline employees who took The Breakroom Quiz
213th of 631 rated colleges and universities
Job description
The University of Mississippi - fondly referred to as Ole Miss - stands as a premier public research institution with a proud legacy of academic distinction. We are devoted to nurturing a vibrant, inclusive community where every member - student, faculty, and staff - can achieve their fullest potential.
Join the Ole Miss Family - Build Your Legacy Here!
Department:
Office for Research & Economic Development
Job Summary:
The Director of Research Compliance provides strategic leadership, regulatory expertise, and administrative oversight for the University's human, animal, and institutional biosafety research compliance programs. Reporting to the Assistant Vice Chancellor for Research Integrity, Security, and Compliance, this position directs the daily administration and continuous improvement of the Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and Institutional Biosafety Committee (IBC) to ensure research involving human participants, laboratory animals, and biological materials is conducted in accordance with applicable federal and state regulations, accreditation standards, sponsor requirements, NIH Guidelines, and University policies.The Director serves as the primary resource for the research enterprise on complex regulatory and ethical issues affecting research compliance. The position develops and implements policies, procedures, and educational initiatives that promote responsible conduct of research while supporting an efficient, service-oriented research environment. The Director oversees post-approval monitoring, investigations, accreditation activities, and regulatory reporting, supervises research compliance personnel, and collaborates with institutional leadership to strengthen the University's research compliance infrastructure through continuous assessment and process improvement.
Job Description:
Essential Functions
- Directs the administration of the Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and Institutional Biosafety Committee (IBC), ensuring compliance with applicable federal regulations, accreditation standards, sponsor requirements, and institutional policies.
- Oversees regulatory review processes for research involving human participants, laboratory animals, recombinant or synthetic nucleic acid molecules, and other regulated research activities.
- Oversees post-approval monitoring, quality assurance activities, and program assessments to evaluate compliance and identify opportunities for program improvement.
- Directs investigations of allegations of noncompliance, protocol deviations, adverse events, animal welfare concerns, biosafety incidents, and other reportable events, including corrective actions and required institutional or regulatory reporting.
- Establishes program priorities, performance expectations, and operational objectives for assigned research compliance programs. Interprets federal regulations, agency guidance, and institutional policy, providing regulatory guidance to investigators, committee members, institutional officials, and University leadership.
- Develops, implements, and periodically evaluates policies, procedures, guidance documents, and standard operating procedures governing research compliance activities.
- Collaborates with institutional stakeholders including the Biological Safety Officer, Attending Veterinarian, Sponsored Programs Administration office, Environmental Health and Safety office, and legal counsel to identify compliance risks, develop institutional policy, and implement strategic initiatives.
- Leads institutional activities related to accreditation, inspections, audits, self-assessments, and external program reviews.
- Develops and delivers education and training programs that promote ethical conduct of research and regulatory compliance.
- Supervises research compliance personnel, including hiring, performance management, professional development, workload distribution, and resource allocation.
- Represents the University in interactions with regulatory agencies, accrediting organizations, sponsors, and professional organizations.
- Performs other duties as assigned.
Preferred Qualifications
- Master's degree or higher in a relevant discipline.
- Experience administering Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and/or Institutional Biosafety Committee (IBC) programs at a research-intensive institution.
- Professional certification such as Certified IRB Professional (CIP), Certified Professional IACUC Administrator (CPIA), Certified Biological Safety Professional (CBSP), or a comparable credential.
- Direct experience in the conduct of research at an academic institution.
- Experience supervising professional staff and managing multiple research compliance programs.
Cover letter and resume required.
Cover letter should be no more than two pages and reflect your own professional experience, judgment, and communication style. Your letter should address the following:
- Your approach to leading compliance programs that must both protect the institution and support the research community.
- One aspect of this position that would represent a meaningful professional challenge or area of growth for you.
Job Responsibilities:
Preferred QualificationsMaster's degree or higher in a relevant discipline.
Experience administering Institutional Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and/or Institutional Biosafety Committee (IBC) programs at a research-intensive institution.
Professional certification such as Certified IRB Professional (CIP), Certified Professional IACUC Administrator (CPIA), Certified Biological Safety Professional (CBSP), or a comparable credential.
Direct experience in the conduct of research at an academic institution.
Experience supervising professional staff and managing multiple research compliance programs.
Education Qualifications:
Bachelor's (Required)Experience:
Relevant experience| 10 Years Experience, 5 Years Supervisory| RequiredCompensation:
$133,827.20 - $200,720.00Interview Requirement:
Interview Requirements: Any candidate who is called for an interview must notify the Department of Equal Opportunity/Regulatory Compliance in writing of any reasonable accommodation needed prior to the date of the interview.
EEO Statement:
The University of Mississippi provides equal opportunity in any employment practice, education program, or education activity to all qualified persons. The University complies with all applicable laws regarding equal opportunity and does not unlawfully discriminate against any employee or applicant for employment based upon race, color, gender, sex, pregnancy, sexual orientation, gender identity or expression, religion, national origin, ethnicity, citizenship, age, disability, military status, protected veteran status, genetic information, or any other legally protected status.
Background Check Statement:
The University of Mississippi is committed to providing a safe campus community. UM conducts background investigations for applicants being considered for employment. Background investigations include a criminal history record check, and when appropriate, a financial (credit) report or driving history check.
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About University of Mississippi
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Industry
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Company size
5,001 - 10,000 Employees
Headquarters location
Oxford, MS, US
Year founded
1844