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Remote Irb Jobs in California (NOW HIRING)

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 ...

Nourish

Research Associate

San Francisco, CA · On-site +1

This role is full-time and open to NYC-based or remote candidates. Our office is located in Gramercy. Key Responsibilities: * Design and execute IRB protocols -- Own prospective study protocols from ...

Nourish

Research Associate

San Diego, CA · On-site +1

This role is full-time and open to NYC-based or remote candidates. Our office is located in Gramercy. Key Responsibilities: * Design and execute IRB protocols -- Own prospective study protocols from ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

... IRB/EC approvals and site files. * Assist in writing and reviewing protocols, informed consent forms (ICFs), and other study-related documents. Clinical Monitoring: * Perform remote monitoring ...

NCIRE

Staff Research Associate II

San Francisco, CA · On-site +1

Administer, pilot, and analyze remote psychophysiological fear-conditioning paradigms , including ... Maintain and organize regulatory documents (IRB submissions, amendments, renewals, consent forms ...

NCIRE

Staff Research Associate II

San Francisco, CA · On-site +1

Administer, pilot, and analyze remote psychophysiological fear-conditioning paradigms , including ... Maintain and organize regulatory documents (IRB submissions, amendments, renewals, consent forms ...

NCIRE

Staff Research Associate I

San Francisco, CA · Remote

Help administer, pilot, and monitor remote psychophysiological fear-conditioning paradigms ... logs) and support IRB-related tasks under the guidance of senior staff. * Communicate ...

ICON

Senior Clinical Research Associate

Los Angeles, CA · On-site +1

$110K - $138K/yr

Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ... Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and ...

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Remote Irb information

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How much do remote irb jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for remote irb in California is $21.22, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $22.55 per hour, depending on experience, location, and employer.

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 a remote IRB job?

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 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.

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 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.

More about Remote Irb jobs

What are the most commonly searched types of Irb jobs in California?

The most popular types of Irb jobs in California are:

What are popular job titles related to Remote Irb jobs in California?

For Remote Irb jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Irb jobs in California look for?

The top searched job categories for Remote Irb jobs in California are:

What cities in California are hiring for Remote Irb jobs?

Cities in California with the most Remote Irb job openings:

Remote Irb jobs near you
Infographic showing various Remote Irb job openings in California as of August 2026, with employment types broken down into 5% As Needed, 90% Full Time, and 5% Part Time. Highlights an 100% Remote job distribution, with an average salary of $44,138 per year, or $21.2 per hour.

Research Analyst (Remote)

Tilda Research

Remote

Full-time

Re-posted 16 days ago

Job description

About the Role

We are looking for candidates with excellent interpersonal and english communication skills, who can work in a Research Analyst role for our company. We are based in India and USA and this position will be fully remote, working from home.


You will have excellent email communication, document parsing and review skills to understand various clinical research related tasks and requirements. Some understanding of basic medical terminology is helpful, but not required. You will be a quick learner, with the ability to learn from online sources and get up to speed on various clinical research related topics like IRB interactions, Study Protocols, Delegation of Authority, inventory logs, etc.


We will provide some domain and job specific context, but we expect you to be able to learn on the job and be self-motivated to perform.


Responsibilities

  • Interact with biotechnology and pharma clients over email and create specific regulatory and supporting documentation as required
  • Manage, fact-check and enter data across various research related systems
  • Respond to any regulatory document requests by looking up the info in our local repository and sending emails back
  • Organize documentation, and get e-Signatures from respective parties if required
  • Any administrative tasks which might come up

Requirements

  • MBA required
  • Excellent internet connection at home with video conference capability
  • Ability to work during late hours (1/2-time overlap with US time zone)
  • Excellent spoken and written english communication
  • Ability to learn and use new technology and software
  • Attention to detail

About Tilda

The Tilda team has held various roles across all aspects of clinical trial management over the years. And during this time, we have often asked questions around clinical trial site management being so.. inefficient, opaque, slow and broken. Our drive to find a solution, and our belief in technology to bridge the gap brought us together to build a new, ground-up network of clinical trial sites, enabled by our technology platform. By investing in workflow automation, centralization and data integration across our sites, we are able to drive better study conduct metrics, and success for our physicians, pharma and CRO partners. We are inviting passionate individuals who can relate to our mission, to join our team of world-class engineers, data scientists and clinical operations experts to reimagine the infrastructure for modern health innovation. We are a San Francisco based startup, backed by leading venture funds and industry leaders.

Employment Type: FULL_TIME

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