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Remote Irb Jobs (NOW HIRING)

Advarra

Sr Editor, Consent Form Development

... remote meeting applications such as Zoom or RingCentral, and web-based proprietary software Preferred Qualifications * 1 year of IRB experience * Experience writing and/or editing consent forms or ...

Tilda Research

We are based in India and USA and this position will be fully remote, working from home. You will ... like IRB interactions, Study Protocols, Delegation of Authority, inventory logs, etc. We will ...

The University of Miami

Regulatory Analyst 1

Miami, FL · On-site +1

Remote option is available for this position. The Regulatory Analyst will be responsible for ... This position requires knowledge of IRB policies and procedures, and Federal Regulations for ...

University of Miami

Regulatory Analyst 1

Miami, FL · On-site +1

Remote option is available for this position. The Regulatory Analyst will be responsible for ... This position requires knowledge of IRB policies and procedures, and Federal Regulations for ...

ARTHREX

Clinical Study Manager (Remote)

OR · Remote

$84K - $110K/yr

Remote Salary Range: Salary Minimum: $84,000.00 Salary Maximum: $110,000.00 Arthrex, Inc. is a ... Facilitate IRB approval at the site and sponsor level. * Oversee and approve site activation ...

New

ARTHREX

Clinical Study Manager (Remote)

Naples, FL · Remote

$84K - $110K/yr

Remote Salary Range: Salary Minimum: $84,000.00 Salary Maximum: $110,000.00 Arthrex, Inc. is a ... Facilitate IRB approval at the site and sponsor level. * Oversee and approve site activation ...

New

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.

Dana-Farber Cancer Institute

$26.25 - $35/hr

May be responsible for site IRB submissions (violations, deviations, severe adverse event reports ... Ability to work across satellite locations and provide on-site and remote support * Is competent ...

Dana-Farber Cancer Institute

This position's work location is fully remote with occasional time on-campus in Boston, MA. The ... Create and maintain tracking for all subsequent submissions to the SRC/IRB; protocol & consent ...

Houston Methodist

... Review Board (IRB), Institutional Animal Care and Use Committee (IACUC), and/or Institutional ... remote/teleconferences, or face-to-face sessions with the entire research team. * Serves as a ...

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How much do remote irb jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for remote irb in the United States is $21.50, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $22.84 per hour, depending on experience, location, and employer.

What are some common challenges faced by Remote IRB Coordinators, and how can they be addressed?

Remote IRB Coordinators often face challenges such as ensuring clear communication with research teams across different locations and time zones, navigating complex regulatory requirements, and maintaining thorough documentation electronically. These challenges can be addressed by leveraging secure collaboration tools, establishing regular check-ins with team members, and staying updated on evolving compliance standards. Developing strong organizational habits and participating in ongoing professional development can also make it easier to manage the demands of a remote IRB role.

What is a Remote IRB?

A Remote IRB, or Institutional Review Board, is a committee that reviews and approves research involving human subjects, but operates remotely rather than in a traditional onsite setting. Remote IRBs allow members to conduct reviews, meetings, and communications online, making the process more flexible and accessible for institutions and researchers across different locations. This setup is especially valuable for multi-site studies or organizations without their own IRB, as it streamlines ethical oversight while ensuring compliance with federal and institutional guidelines.

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

AspectRemote IrbRemote Clinical Research Coordinator
Required CredentialsIRB approval, research ethics knowledgeClinical research experience, regulatory knowledge
Work EnvironmentReview boards, ethics committees, administrativeStudy sites, patient interaction, data management
Employer & Industry UsageHospitals, research institutions, biotech firmsPharmaceutical companies, CROs, hospitals
Common Search & ComparisonYesNo

The Remote Irb role focuses on reviewing research protocols for ethical compliance, requiring knowledge of research ethics and IRB procedures. In contrast, a Remote Clinical Research Coordinator manages study operations, patient recruitment, and data collection. While both roles are integral to clinical research, they differ in responsibilities, credentials, and work environment.

What Are Remote IRB Jobs?

Remote IRB jobs include work as a remote IRB administrator, a remote IRB analyst, and a remote IRB coordinator. Your responsibilities and duties differ depending on your specific position. For example, a remote IRB analyst performs analysis and is responsible for assessing whether or not a study meets all the guidelines and regulatory requirements for the safety and welfare of human subjects. As a remote IRB coordinator, your role is to coordinate internal review board research and compliance during studies. This includes ensuring that test subjects received the proper paperwork and release forms and that studies remain on schedule. You can work from home in any of these positions.

What are the key skills and qualifications needed to thrive as a Remote IRB (Institutional Review Board) Coordinator, and why are they important?

To thrive as a Remote IRB Coordinator, you typically need a background in research ethics, regulatory compliance, and a degree in a related field such as health sciences or public administration. Familiarity with IRB management systems, federal regulations (such as 45 CFR 46), and certifications like CIP (Certified IRB Professional) are often required. Exceptional attention to detail, organizational skills, and effective remote communication are vital soft skills for this role. These competencies are crucial for ensuring ethical research practices, regulatory compliance, and efficient coordination in a remote environment.
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What cities are hiring for Remote Irb jobs? Cities with the most Remote Irb job openings:
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Remote Irb jobs near you
Infographic showing various Remote Irb job openings in the United States as of June 2026, with employment types broken down into 79% Full Time, 19% Part Time, and 2% Contract. Highlights an 100% Remote job distribution, with an average salary of $44,724 per year, or $21.5 per hour.
Sr Editor, Consent Form Development

Sr Editor, Consent Form Development

Advarra

Remote

Full-time

Medical

Posted yesterday

Job description

Company Information
At Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials.
Company Culture
Our employees are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each employee is not only valued but empowered to thrive and make a meaningful impact.
Job Overview Summary
Supports the IRB Services department in the review of incoming submissions and preparation of informed consent forms (ICFs) used in the conduct of human subjects research. In addition, the Senior Editor may mentor new editors and complete projects as defined by management.
Job Duties & Responsibilities
  • Conduct an accurate pre-review of new and revised consent forms in regulatory compliance with applicable FDA, HHS, Health Canada, TCPS2 regulations, ICH GCP guidance, and operational compliance with Advarra Standard Operating Procedures and Work Instructions

  • Edit new and revised consent forms to ensure regulatory compliance and alignment with Advarra operational standards

  • Apply negotiated Sponsor and site language to consent form documents as required by client agreements documented in mandatory language documents or MLD's

  • Collaborate with Board members and staff to include all necessary edits to the consent form from the various stakeholders

  • Complete informed consent quality control check for yourself and others

  • Mentor new team members, as requested

  • Maintain and increase individual regulatory knowledge to assist with organizational compliance:

  • Maintain and increase knowledge of U.S. and/or Canadian Regulations and Guidelines in the area of Human Subject Protections, drug research, device research, and cosmetic research

  • Complete standard Human Subjects Research Training, such as CITI, on a repeating cycle determined by management

  • Complete organizational training as required by management

  • Attend one IRB meeting per month to enhance knowledge and understanding of IRB processes (two meetings per month during the initial training period)

  • Offer process improvement suggestions to management, as applicable

  • Other duties as assigned

Location
This role is open to candidates working remotely in the United States.
Basic Qualifications
  • Minimum of 2 years of experience in technical/medical writing and/or editing in addition to a Bachelor's degree

  • Experience writing and/or editing consent forms or other research documents

  • Proficiency in Word processing and editing (including use of Tracked Changes and Compare Merge functions)

  • Familiar with Excel, PowerPoint, direct messaging applications such as Slack, remote meeting applications such as Zoom or RingCentral, and web-based proprietary software

Preferred Qualifications
  • 1 year of IRB experience

  • Experience writing and/or editing consent forms or other research documents

  • Certified IRB Professional (CIP) or completion of CIP within two (2) years of eligibility

  • Ability to communicate clearly and professional in English, both verbal and written skills

  • Excellent interpersonal skills to work professionally and effectively with others and provide high levels of customer service

  • In-depth knowledge of matters regarding human subjects research and informed consent

  • Familiar with scientific/medical terminology and able to convert scientific/medical information to lay terms

  • Ability to edit technical and/or medical documents

  • Ability to read and comprehend advanced technical/medical documents such as medical protocols and informed consent forms

  • Ability to manage various editing projects under conflicting demands and priorities

  • Dependably produces high quality work

  • Must have high level of attention to detail, accuracy and thoroughness; problem solving skills

  • Ability to follow written and verbal instructions and work independently as required

Physical and Mental Requirements
  • Sit or stand for extended periods of time at stationary workstation

  • Regularly carry, raise, and lower objects of up to 10 Lbs.

  • Learn and comprehend basic instructions

  • Focus and attention to tasks and responsibilities

  • Verbal communication; listening and understanding, responding, and speaking

Advarra is an equal opportunity employer that is committed to providing a workplace that is free from discrimination and harassment of any kind based on race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions, sexual orientation, and gender identify), national origin, age, disability or genetic information or any other status or characteristic protected by federal, state, or local law.
Pay Transparency Statement
The base salary range for this role is $66,767 - $116,089. Note that salary may vary based on location, skills, and experience and may vary from the amounts listed above. This position may also be eligible for a variable bonus in addition to base salary as well as health coverage, paid holidays, and other benefits.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
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About Advarra

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

201 - 500 Employees

Headquarters location

Columbia, MD, US

Year founded

1983

Social media

Twitter

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