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Remote Irb Analyst Jobs in California (NOW HIRING)

... Analyst role for our company. We are based in India and USA and this position will be fully remote ... like IRB interactions, Study Protocols, Delegation of Authority, inventory logs, etc. We will ...

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

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

... logs) and support IRB-related tasks under the guidance of senior staff. * Communicate ... analysis (e.g., Biopac , LSL , EDA, EMG, HR/HRV, facial coding, remote PPG from video); prior ...

... IRB/EC submissions with follow-thorough to ensure successful progress * Responsible for ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

... IRB/EC submissions with follow-thorough to ensure successful progress * Responsible for ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

This is a hybrid-remote role, with the expectation to work from our San Francisco offices at least ... Plan, conduct, and analyze a range of user research studies, including ethnographic studies ...

... IRB/EC submissions with follow-thorough to ensure successful progress * Accountable for ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

... IRB/EC submissions with follow-thorough to ensure successful progress * Accountable for ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

... IRB/EC submissions with follow-thorough to ensure successful progress * Accountable for ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

... IRB/EC submissions with follow-thorough to ensure successful progress * Accountable for ... Perform on-site and remote site qualification visits, site initiation visits, interim monitoring ...

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.

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

The most popular types of Irb Analyst jobs in California are:

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

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

What cities in California are hiring for Remote Irb Analyst jobs?

Cities in California with the most Remote Irb Analyst job openings:

Infographic showing various Remote Irb Analyst job openings in California as of July 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 100% Remote job distribution.

Full-time

Re-posted 11 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