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Irb Part Time Remote Jobs (NOW HIRING)

Aegis Ventures

Clinical Affairs Manager (Part-Time)

$135 - $175/hr

This is a part-time position (approximately 25 hours per month) and is remote within the U.S., with ... Support hospital IRB processes and vendor vetting procedures * Lead clinical training and education ...

The Pennsylvania State University

$18/hr

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Recruit, screen, and schedule participants according to IRB-approved procedures * Describe study ...

The Pennsylvania State University

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Familiarity with research procedures, IRB compliance, or school-based intervention studies.

The Pennsylvania State University

$16 - $22/hr

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Penn State student * Have or will be completing IRB-certification * Have strong written ...

The Pennsylvania State University

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Board (IRB) training. Knowledge of learning theories, instructional theories, or advanced ...

Unf

Part-Time Research Associate

Jacksonville, FL · On-site +1

$35/hr

Familiarity with program evaluation methods and IRB processes. * Previous involvement in innovation ... Hybrid and remote work options may be available depending on project needs. * Compensation ...

Aptive

Management Analyst

... g., FDA, IRB, NIH, VA). This is 100% remote position, with an option as either full-time or part-time. Primary Responsibilities * Provide administrative and programmatic support for a VA field ...

Aptive

Management Analyst

... g., FDA, IRB, NIH, VA). This is 100% remote position, with an option as either full-time or part-time. Primary Responsibilities * Provide administrative and programmatic support for a VA field ...

The Pennsylvania State University

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... This person is responsible for completing all documents necessary for continuing IRB approval, the ...

University of Utah

Hourly Research Assistants

Campus, IL · Remote

$20/hr

This position is remote friendly. For applicants residing outside of Utah, additional approvals ... Supporting IRB submissions, amendments, and regulatory documentation * Literature searches, article ...

University of Utah

UU Student - Research

Campus, IL · Remote

$20/hr

This position is remote-friendly. For applicants residing outside of Utah, additional approvals ... Supporting IRB submissions, amendments, and regulatory documentation * Literature searches, article ...

University of Utah

Hourly Research Assistants

Campus, IL · Remote

$20/hr

This position is remote friendly. For applicants residing outside of Utah, additional approvals ... Supporting IRB submissions, amendments, and regulatory documentation * Literature searches, article ...

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Irb Part Time Remote information

What are the key skills and qualifications needed to thrive as an IRB (Institutional Review Board) Part-Time Remote professional, and why are they important?

To thrive as an IRB Part-Time Remote professional, you need a solid understanding of research ethics, regulatory compliance, and human subjects protection, often supported by experience in clinical research or a related field. Familiarity with IRB management systems, federal regulations (like the Common Rule), and completion of relevant certifications such as CITI training is typically required. Strong attention to detail, effective written communication, and time management are crucial soft skills for reviewing protocols and collaborating remotely. These skills ensure ethical oversight of research activities, regulatory adherence, and efficient operation in a remote, part-time environment.

How do part-time remote IRB professionals typically collaborate with on-site team members and researchers?

Part-time remote IRB professionals often use virtual collaboration tools such as email, video conferencing, and secure document management systems to communicate with on-site team members and researchers. Regular virtual meetings are scheduled to review protocols, discuss ethical concerns, and ensure compliance with regulatory standards. Clear communication and strong organizational skills are essential, as remote IRB members must coordinate with both the IRB chair and administrative staff to maintain workflow and meet review deadlines. Many institutions provide robust onboarding and ongoing support to help remote IRB members stay connected and effective in their roles.

What are IRB part-time remote jobs?

IRB part-time remote jobs involve working for an Institutional Review Board (IRB) on a part-time basis from a remote location. These roles typically include tasks such as reviewing research protocols, ensuring compliance with ethical standards, and protecting the rights and welfare of research participants. Positions may include IRB reviewers, coordinators, or administrative staff. Working remotely allows for flexible scheduling and the ability to contribute expertise from various locations. These jobs often require knowledge of research ethics, regulatory guidelines, and strong communication skills.

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

AspectIrb Part Time RemoteClinical Research Coordinator
CredentialsTypically requires IRB certification, research ethics knowledgeRequires clinical research experience, sometimes certifications like CCRP
Work EnvironmentRemote, flexible hours, independent tasksOften on-site or hybrid, coordinating clinical trials
Employer & IndustryResearch institutions, biotech, pharmaHospitals, research centers, pharma companies

While both roles involve research oversight, Irb Part Time Remote focuses on ethical review and compliance remotely, whereas Clinical Research Coordinators manage and oversee clinical trials on-site or in hybrid settings. The roles share certifications and industry overlap but differ mainly in work environment and specific responsibilities.

More about Irb Part Time Remote jobs
What cities are hiring for Irb Part Time Remote jobs? Cities with the most Irb Part Time Remote job openings:
What are the most commonly searched types of Irb Remote jobs? The most popular types of Irb Remote jobs are:
What states have the most Irb Part Time Remote jobs? States with the most job openings for Irb Part Time Remote jobs include:
What job categories do people searching Irb Part Time Remote jobs look for? The top searched job categories for Irb Part Time Remote jobs are:
Irb Part Time Remote jobs near you
Infographic showing various Irb Part Time Remote job openings in the United States as of May 2026, with employment types broken down into 2% As Needed, 94% Full Time, 2% Temporary, and 2% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.
IRB ANALYST II

IRB ANALYST II

Cooper University Health Care

Camden, NJ • Remote

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement

Posted 14 days ago

Cooper University Health Care rating

7.5

Company rating: 7.5 out of 10

Based on 129 frontline employees who took The Breakroom Quiz

217th of 864 rated healthcare providers

Job description

About us

At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. We have a commitment to our employees to provide competitive rates and compensation programs.  Cooper offers full and part-time employees a comprehensive benefits program, including health, dental, vision, life, disability, and retirement. We also provide attractive working conditions and opportunities for career growth through professional development.

Discover why Cooper University Health Care is the employer of choice in South Jersey.


Short Description

FULLY REMOTE POSITION

The IRB Analyst II will coordinate and attend all IRB and Executive Committee meetings; assist research investigators and study coordinators in the processing of research proposals; review and track new protocol submissions, amendments, adverse event reports, and progress reports; distribute research protocols to administration for review and signatures; notify investigators about impending study expiration; manage and maintain the online electronic system. 
Briefly explain the job’s overall objective:
The IRB Analyst II will coordinate and attend all IRB and Executive Committee meetings; assist research investigators and study coordinators in the processing of research proposals; review and track new protocol submissions, amendments, adverse event reports, and progress reports; prepare and distribute review materials, and agendas and minutes of IRB meetings to all IRB members; generate correspondence to investigators based on determinations made by and assigned expedited reviewer or the Board; distribute research protocols to administration for review and signatures; notify investigators about impending study expiration; manage and maintain the online electronic system and study files (online and/ or paper) that document protocol activity; provide guidance and consultation to IRB members and investigators regarding implementation of federal regulations, state law, and Cooper IRB policies and procedures; and assist the IRB Manager and the IRB Chairs with special assignments. 

The IRB Analyst II will independently review submissions to determine Not Human Subjects Research (NHSR) status or eligibility for Exempt review in accordance with federal regulations and institutional policies. Conduct pre-reviews of expedited studies to ensure completeness, assess risk level. Identify required revisions, provide clear guidance to investigators, and ensure accurate documentation and timely processing within the IRB system.

The IRB Analyst II will conduct limited local context review of studies ceded to external IRBs, as needed. Assist with tracking and maintaining reliance agreements and related records in coordination with the IRB Reliance Manager. Support review of external IRB studies, including pre-reviewing continuing reviews and amendments, to ensure institutional requirements are met and documentation is complete.


Experience Required

Knowledge of the Common Rule (45 CFR 46), FDA regulations, ICHGood Clinical Practice Guidelines, and other relevant requirements and guidelines related to the ethical study of human research subjects.


Education Requirements

A bachelor’s degree in an appropriate field or an equivalent combination of education and experience.
Minimum of 2 years of experience in IRB administration, clinical research, or regulatory compliance with human subjects.

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