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Remote Irb Analyst Jobs (NOW HIRING)

Clinical Research Associate

Boston, MA · On-site +1

$20.16 - $29.01/hr

... analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching ... This position involves working with clinical teams, Institutional Review Boards (IRB), clinical ...

Clinical Research Associate

Boston, MA · Remote

$20.16 - $29.01/hr

... analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching ... This position involves working with clinical teams, Institutional Review Boards (IRB), clinical ...

This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...

This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...

Research Audiologist

$105K - $135K/yr

Remote (U.S.) with periodic travel - Personnel may perform work remotely from their residence ... Support execution of IRB-approved research protocols. * Conduct advanced audiometric and functional ...

... analyses, and recommendations for ongoing and proposed human performance research * Utilize ... IRB, HRPO, IACUC, IBC, MOU, and data-sharing agreements, while ensuring compliance through audit ...

$105K - $135K/yr

Remote (U.S.) with periodic travel - Personnel may perform work remotely from their residence ... Support execution of IRB-approved research protocols. * Conduct advanced audiometric and functional ...

... analytical solutions -we are modernizing clinical trials and accelerating the development of life ... Independently completes IRB/EC submissions for sites or submits to central IRB/EC on behalf of the ...

Remote Schedule: Full-time, 8am - 5pm EST Monday - Friday Salary Range: 58,600.00 - 85,000.00 ... Conduct initial IRB and PRA/OMB screening for research-like activities and prepare documentation ...

$66K - $116K/yr

Job Overview Summary This role conducts Quality Control (QC) activities on complex IRB and staff ... Serves as a resource for process or workflow problem-solving, including root cause analysis and ...

Job Overview Summary This role conducts Quality Control (QC) activities on complex IRB and staff ... Serves as a resource for process or workflow problem-solving, including root cause analysis and ...

Showing results 21-40

Remote Irb Analyst information

What is a remote IRB analyst?

Remote IRB analysts are professionals who review research proposals to ensure they comply with ethical standards and federal regulations, working from a remote location rather than on-site. They are responsible for evaluating study protocols, informed consent documents, and safeguarding the rights and welfare of research participants. Remote IRB analysts typically collaborate with researchers, institutional review boards, and regulatory bodies via digital platforms. This role requires strong attention to detail, knowledge of ethical guidelines, and effective communication skills.

What are the key skills and qualifications needed to thrive as a remote IRB analyst?

To thrive as a Remote IRB Analyst, you need a solid understanding of federal regulations, ethical principles in human subjects research, and experience with IRB processes, often supported by a relevant degree. Familiarity with electronic IRB management systems and certifications such as CIP (Certified IRB Professional) are commonly required. Excellent organizational skills, attention to detail, and strong written communication are essential soft skills for this role. These competencies ensure ethical compliance, efficient review processes, and effective collaboration in protecting research participants.

How does a remote IRB analyst typically collaborate with research teams and other stakeholders?

As a Remote IRB Analyst, you will regularly interact with research coordinators, principal investigators, and institutional officials primarily through virtual meetings, email, and specialized IRB management platforms. Clear communication and timely feedback are essential, as you’ll review research protocols, provide guidance on regulatory compliance, and address queries about ethical standards. Successful analysts proactively coordinate with team members to resolve issues, ensure documentation accuracy, and maintain workflow efficiency, despite working from different locations.

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

AspectRemote Irb AnalystRemote Clinical Research Coordinator
Required CredentialsIRB certification, research ethics knowledgeClinical research experience, sometimes certifications
Work EnvironmentRemote, primarily administrative and review tasksRemote or onsite, coordinating clinical trial activities
Employer & IndustryResearch institutions, biotech, pharmaHospitals, research sites, pharma companies
Common Search & ComparisonYesYes

The Remote Irb Analyst primarily reviews and approves research protocols to ensure ethical compliance, requiring IRB certification. In contrast, the Remote Clinical Research Coordinator manages trial logistics and participant coordination. Both roles are essential in clinical research but differ in responsibilities and focus areas.

More about Remote Irb Analyst jobs

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What are the most commonly searched types of Irb Analyst jobs?

The most popular types of Irb Analyst jobs are:

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Infographic showing various Remote Irb Analyst job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% Remote job distribution.

$68K - $70K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 9 days ago


Job description

Job Description:

Job Description:

AboutTheChicago School

The Chicago Schoolis a nonprofit university with seven in-person locations across the United States, a growing online campus, and education partnerships worldwide. The Chicago School is a minority-majority university with 6,000+ students across 35+ degree programs in psychology, behavioral health, and nursing.The Chicago School is committed to creating a diverse pipeline offuture professionals who will fundamentally improve the health and well-being of future generations of diverse communities.Founded in 1979 by a group of psychologists and educators, The Chicago School has grown into a dominant and globally respected leader in the fields of psychology and behavioral health sciences. Today, The Chicago School has an annual operating budget of nearly $150M and employs nearly 600 full-time faculty and staff. As an institution, The Chicago School is deeply committed to student success, innovation, and community impact. Our students are meaningfully connected in their communities, donating more than 1.2 million service hours per year through fieldwork and practicum opportunities.The Chicago School is part of the TCS Education System, a nonprofit system of colleges advancing student success and community impact.

Position Summary:

The Research Compliance Specialist provides comprehensive support for the institution's research compliance program, including compliance monitoring and education and training. The Specialist will conduct compliance assessments, support audits, and partner with academic and administrative units to promote research integrity and accountability. The Specialist will also develop and deliver human research protections training for faculty, staff, and students and create educational materials, coordinate workshops and webinars, and partner with academic units to strengthen ethical research practices throughout the institution. This role serves as a key resource for faculty, staff, and external partners, ensuring adherence to federal regulations, institutional policies, and best practices in human subjects research.

Principal Duties & Responsibilities:

Research Compliance Monitoring & Auditing

  • Conduct for-cause audits authorized by the IRB or institutional official.
  • Conduct periodic compliance reviews of research protocols and documentation.
  • Write reports and communicate findings with investigators, committees, and appropriate parties.
  • Monitor adherence to IRB determinations, continuing review obligations, and reporting requirements.
  • Support internal audits relating to research governance.
  • Identify potential compliance gaps and recommend corrective action.
  • Collaborate with IRB and sponsored programs offices to maintain compliance frameworks.

Education & Training

  • Design and implement training programs on IRB submission processes, federal regulations, and best practices in human subject protections for both socio-behavioral and biomedical research.
  • Develop written and multimedia resources (guides, FAQs, webinars).
  • Partner with departments to offer tailored training sessions and support.
  • Track training participation and recommend improvements to curricula.
  • Stay current with regulatory changes and emerging trends in research compliance education.
  • Other responsibilities as assigned by the IRB Director.

Required Qualifications:

  • Bachelor's degree in relevant field (e.g., research compliance, public health, social sciences, etc.) and 3 years relevant program experience.
  • Experience with human subjects research, IRB operations, research compliance, education and training.
  • Familiarity with compliance auditing or monitoring practices.
  • Knowledge of federal regulations governing research and institutional policies.
  • Strong analytical, organizational, and documentation skills.
  • Experience developing training programs or educational materials.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple priorities and work independently.
  • Strong interpersonal skills with a collaborative and service-oriented approach.
  • Discretion and professionalism in handling sensitive information.
  • Proficiency with Microsoft Office and electronic research/compliance systems.
  • Comfortable working in a fully remote environment using tools such as Zoom.

Preferred Qualifications:

  • Experience in higher education or academic research administration.
  • Experience using Cayuse.
  • Certification in research or compliance (e.g., CIP, CCRC, CIM, CHRC, CUNY, RCI).

Compensation & Benefits:

This opportunity is budgeted at $68,000-$70,000 base compensation. Additional compensation factors may impact total compensation. To learn more about our competitive benefits and additional rewards, including generous paid time-off, medical and dental insurance coverage, life and disability insurance, retirement plan with employer contribution, multiple flexible spending accounts, tuition reimbursement, click the link below.

https://www.thechicagoschool.edu/career-opportunities/

The Chicago School is an Equal Opportunity Employer.

The Chicago School offers a generous compensation and benefits package, as well as the opportunity to work for a leader in the field of education. Some of our key benefits include: generous paid time-off, medical and dental coverage, company-paid life and disability insurance, retirement plan with employer contribution, multiple flexible spending accounts (FSA), tuition reimbursement, professional development, and regular employee appreciation events.The Chicago School is an Equal Opportunity Employer.

Apply Link:

Company:

The Chicago School