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Irb Post Approval Monitor Jobs (NOW HIRING)

This role manages major compliance areas-including IRB, IACUC, biosafety/biosecurity, conflict of ... The position conducts regulatory reviews, audits, inspections, and post-approval monitoring to ...

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Irb Post Approval Monitor information

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How much do irb post approval monitor jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for irb post approval monitor in the United States is $16.01, according to ZipRecruiter salary data. Most workers in this role earn between $14.66 and $17.31 per hour, depending on experience, location, and employer.

What are some typical challenges faced by an IRB Post Approval Monitor, and how can they be effectively managed?

IRB Post Approval Monitors often encounter challenges such as navigating complex regulatory requirements, managing high volumes of ongoing studies, and ensuring timely communication with research teams. Staying organized and maintaining up-to-date documentation are essential for effective monitoring. Building collaborative relationships with investigators and leveraging electronic tracking systems can help streamline the process and ensure compliance with IRB protocols.

Is a principal investigator required to comply with the Institutional Review Board IRB?

Yes, a principal investigator (PI) is required to comply with IRB regulations, as they are responsible for ensuring that research involving human subjects adheres to ethical standards and federal guidelines. The PI must obtain IRB approval before starting the study and follow all approved protocols throughout the research process.

What is the difference between Irb Post Approval Monitor vs Clinical Research Coordinator?

AspectIrb Post Approval MonitorClinical Research Coordinator
CertificationsOften requires IRB-related certifications, research compliance trainingRequires Good Clinical Practice (GCP) training, sometimes certifications
Work EnvironmentMonitoring research sites post-approval, ensuring complianceManaging daily clinical trial activities, participant coordination
Employer & IndustryResearch institutions, hospitals, biotech firmsHospitals, research centers, pharmaceutical companies

The Irb Post Approval Monitor focuses on overseeing research compliance after IRB approval, ensuring protocols are followed. In contrast, a Clinical Research Coordinator manages the day-to-day operations of clinical trials, including participant recruitment and data collection. Both roles are vital in clinical research but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as an IRB Post Approval Monitor, and why are they important?

To thrive as an IRB Post Approval Monitor, you need a strong understanding of research compliance, federal regulations (such as the Common Rule), and human subjects protection, usually supported by a relevant bachelor's or advanced degree. Familiarity with research management systems, compliance tracking software, and certifications like CIP (Certified IRB Professional) are often required. Strong attention to detail, analytical thinking, and effective communication skills set outstanding monitors apart. These competencies ensure ethical oversight, regulatory adherence, and the protection of research participants throughout the study lifecycle.

What is an IRB assistant?

An IRB assistant supports Institutional Review Board (IRB) activities by managing documentation, coordinating communication between researchers and IRB members, and ensuring compliance with ethical guidelines. They often handle administrative tasks, prepare submission materials, and maintain records to facilitate the review process.

Is clinical research coordinator a stable job?

A clinical research coordinator role is generally considered stable, especially in institutions with ongoing research projects and regulatory compliance requirements. The job often offers regular hours, opportunities for advancement, and may require certifications like CCRC, contributing to job security in the healthcare and research sectors.

What is an IRB Post Approval Monitor?

An IRB Post Approval Monitor is a professional who oversees research studies after they have been approved by an Institutional Review Board (IRB). Their main role is to ensure that studies continue to comply with ethical standards, regulatory requirements, and approved protocols throughout their duration. They conduct routine and for-cause site visits, review study documentation, observe study procedures, and provide education to research staff. This monitoring helps protect research participants and maintains the integrity of the research process.

What is an IRB specialist?

An IRB specialist is a professional responsible for managing and overseeing research protocols to ensure compliance with Institutional Review Board (IRB) regulations. They review study submissions, monitor ongoing research, and ensure ethical standards are maintained, often requiring knowledge of federal guidelines and good clinical practice. This role supports the protection of human research participants and may involve documentation, communication with researchers, and regulatory reporting.
Infographic showing various Irb Post Approval Monitor job openings in the United States as of June 2026, with employment types broken down into 80% Full Time, and 20% Part Time. Highlights an 100% In-person job distribution, with an average salary of $33,308 per year, or $16 per hour.
Regulatory Compliance Cord- Institutional Review Board

Regulatory Compliance Cord- Institutional Review Board

Augusta University Medical Center

Augusta, GA • On-site

$52K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 17 days ago


Job description

*
About Us
Augusta University is Georgia's innovation center for education and health care, training the next generation of innovators, leaders, and healthcare providers in classrooms and clinics on four campuses in Augusta and locations across the state. More than 12,000 students choose Augusta for educational opportunities at the center of Georgia's cybersecurity hub and experiential learning that blends arts and application, humanities, and the health sciences. Augusta is home to Georgia's only public academic health center, where groundbreaking research is creating a healthier, more prosperous Georgia, and world-class clinicians are bringing the medicine of tomorrow to patient care today. Our mission and values https://www.augusta.edu/about/mission.php make Augusta University an institution like no other.
Augusta University's distinct characteristics in education and research include real-world experiences and community engagement, as well as a culture of building community, corporate and government partnerships that address health, security, economic and societal concerns locally and across the state.
The University System of Georgia https://www.usg.edu/hr/orientation/welcome_to_the_board_of_regents_university_system_office is comprised of our 26 institutions of higher education and learning as well as the System Office. Our USG Statement of Core Values are Integrity, Excellence, Accountability, and Respect. These values serve as the foundation for all that we do as an organization, and each USG community 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 Policy 8.2.18.1.2 and can be found online at https://www.usg.edu/policymanual/section8/C224/#p8.2.18_personnel_conduct.
Additionally, USG supports Freedom of Expression as stated in Board Policy 6.5 Freedom of Expression and Academic Freedom found online at https://www.usg.edu/policymanual/section6/C2653 .
Location
Augusta University
Our Health Sciences Campus: 1120 15th Street, Augusta, GA 30912
Our Summerville Campus: 2500 Walton Way, Augusta, GA 30904
College/Department Information
The Institutional Review Board Office ensures the research goals of the Augusta University enterprise are met, while protecting human subjects involved in research and verifying the enterprise meets compliance standards. The IRB Office also serves as the central contact for facilitating the goals of the Enterprise Human Research Protection Program (HRPP). Our office provides: Administrative support for the internal IRBs and a liaison for the external IRBs; Monitoring and oversight for all IRB approved studies; Education and training for human research investigators, staff, and IRB members.
Job Summary
Supports human research protections program by performing post approval monitoring and quality assurance activities of research faculty, staff, students, as well as the internal IRBs (3).
Responsibilities
R esponsibilities to include, but are not limited to:
Conduct routine, rotational, and for-cause audits of research studies involving human subjects and investigate possible research non-compliance. Prepare for and provide on-site assistance with external audits and institutional site visits.
Conduct quality assessments of internal IRB submissions prior to release of IRB approvals to ensure compliance with federal/institutional regulations and AAHRPP accreditation guidelines and to identify areas of improvement for IRB administrators.
Provide research compliance training when required for study startup, as part of the audit corrective actions, and other times as deemed necessary.
Perform all other job-related duties as assigned.
Required Qualifications
Bachelor's degree from an accredited college or university and a minimum of two years of experience as a clinical research coordinator, monitor, or IRB professional.
Preferred Qualifications
Bachelor's degree from an accredited college or university preferably in a research, scientific or related technical field or training in a research area.
Active engagement in clinical research evaluation that demonstrates leadership and ability to manage a variety of professionals.
Knowledge, Skills, & Abilities
KNOWLEDGE
Proficient in Microsoft Office and other computer software/databases.
SKILLS
Excellent interpersonal, written, and verbal communication skills.
Detail oriented with strong multi-tasking skills.
ABILITIES
Ability to maintain confidentiality.
Shift/Salary/Benefits
Shift: Days; Monday - Friday (Work outside of normal business hours may be required).
Salary Minimum: $52,500 annually.
Pay Band: B10
Salary to be commensurate with qualifications of the selected candidate within the established range (generally minimum-midpoint) of the position.
Recruitment Period: Until Filled.
Augusta University offers a variety of benefits to full-time benefits-eligible employees and some of our half-time (or more) employees.
Benefits that may be elected could include health insurance, dental insurance, life insurance, Teachers Retirement System (or Optional Retirement Plan), as well as earned vacation time, sick leave, and 13 paid holidays.
Also, our full-time employees who have been employed with us successfully for more than 6 months can be considered for the Tuition Assistance Program. Consider applying with us today!
Conditions of Employment
All selected candidates are required to successfully pass a Background Check review prior to starting with Augusta University.
If applicable for the specific position based on the duties: the candidate will also need to have a credit check completed for Positions of Trust and or approved departmental Purchase Card usage.
Motor vehicle reports are required for positions that are required to drive an Augusta University vehicle.
For Faculty Hires: Final candidates will be required to provide proof of completed academic degree(s) as well as post-secondary coursework in the form of original transcript(s). Those candidates trained by a foreign institution will also be required to provide an educational/credential evaluation.
All employees are responsible for ensuring the confidentiality, availability, and integrity of sensitive [patient, student, employee, financial, business, etc.] information by exercising sound judgment and adhering to cybersecurity and privacy policies during their employment and beyond.
Other Information
This position is also responsible for promoting a customer-friendly environment and providing superior service to our patients, students, faculty, and employees. "Augusta University is a patient-and family-centered care institution, where employees partner every day with patients and families for success."
Augusta University is a tobacco-free environment, and the use of any tobacco products on any part of the campus, both inside and outside, is strictly prohibited.
Equal Employment Opportunity
Augusta University is proud to be an equal opportunity employer welcoming applicants from underrepresented groups, including individuals with disabilities and veterans.
How To Apply
Consider applying with us today!
https://www.augusta.edu/hr/jobs/ Search for Job ID: 293037.
Select University Faculty & Staff > External Applicants if you are a candidate from outside the university.
Select University Faculty & Staff > Internal Applicants if you are a current university employee.
If you need further assistance, please contact us at 706-721-9365.