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Irb Analyst Jobs in California (NOW HIRING)

UC Davis Health

Clinical Research Analyst 4

Sacramento, CA · On-site

$99K - $186K/yr

Experience interpreting clinical research protocols, FDA regulations, ICH-GCP guidelines, IRB ... Advanced analytical and critical thinking skills to interpret complex protocols, assess regulatory ...

Tilda Research

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

Amat

Sr. Finance Portfolio Analyst (B4)

Santa Clara, CA · On-site +1

$133K - $183K/yr

Contribute financial analysis and recommendations for Strategic Reviews (SR), EPR, IRB, and AOP processes. Stakeholder Partnership & Team Collaboration * Coordinate with nearshore finance resources ...

23andme

Senior Security Analyst

Palo Alto, CA

$110K - $140K/yr

23andMe Research Institute is looking for an experienced Senior Security Analyst to join our ... IRB) regulated under the 'Common Rule' (45 CFR part 46). More information is available at www ...

23andMe, Inc.

Senior Security Analyst

Palo Alto, CA · On-site

$110 - $140/hr

... Analyst to join our Security Operations team. In this role you will lead security incident response ... IRB) regulated under the 'Common Rule' (45 CFR part 46). More information is available at* www ...

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How much do irb analyst jobs pay per year?

As of Aug 26, 2026, the average yearly pay for irb analyst in California is $72,302.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,800.00 and $85,900.00 per year, depending on experience, location, and employer.

What is an IRB analyst?

An IRB (Institutional Review Board) Analyst is responsible for reviewing research proposals to ensure they comply with ethical guidelines and regulatory requirements for human subjects' protection. They assess study protocols, verify informed consent procedures, and ensure adherence to federal and institutional policies. IRB Analysts collaborate with researchers to address compliance issues and provide guidance on ethical research practices. Their role is critical in safeguarding participants' rights and welfare while facilitating ethical research.

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

To thrive as an IRB Analyst, you need a strong background in research ethics, regulatory compliance, and an understanding of human subjects research, often supported by a relevant bachelor's or master's degree. Familiarity with electronic protocol management systems, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are highly valued. Strong attention to detail, analytical thinking, and effective communication skills set outstanding IRB Analysts apart. These qualities are crucial to ensure thorough, ethical review of research protocols and strict adherence to regulatory standards, protecting the rights and welfare of research participants.

What are some common challenges faced by IRB analysts in their daily work?

IRB Analysts frequently navigate complex regulatory requirements while reviewing a diverse range of research protocols, which can present challenges in interpreting guidelines and ensuring full compliance. They must balance efficiency with thoroughness, often working under tight deadlines to support both researchers and institutional standards. Staying current with evolving ethical standards and federal regulations is essential, as is effectively communicating decisions to investigators who may have varying levels of experience. Despite these challenges, the IRB Analyst role is rewarding for those who value ethical oversight and enjoy collaborative, detail-oriented work.

What do you need to be an IRB analyst?

To become an IRB analyst, candidates typically need a bachelor's degree in a related field such as healthcare, research, or ethics, along with experience in research compliance or regulatory environments. Knowledge of federal regulations like the Common Rule and Good Clinical Practice (GCP) is essential, and certifications such as the Certified IRB Professional (CIP) can enhance qualifications. Strong attention to detail, analytical skills, and the ability to review research protocols are also important for the role.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements set by Institutional Review Boards. They evaluate study procedures, consent forms, and risk assessments, often using specialized software, to protect research participants and maintain compliance. IRB analysts typically have a background in research ethics, healthcare, or related fields and work closely with researchers and regulatory bodies.

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

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Irb Analyst jobs near you
Infographic showing various Irb Analyst job openings in California as of August 2026, with employment types broken down into 84% Full Time, 10% Part Time, and 6% Contract. Highlights an 79% Physical, 8% Hybrid, and 13% Remote job distribution, with an average salary of $72,302 per year, or $34.8 per hour.

Senior Administrative Services Manager (IRB Administrator)

San Diego, CA • On-site

VENESCO, LLC
51 - 200 employees
Learn more about VENESCO, LLCexternal

Full-time

Re-posted 11 days ago

Job description

Description


Location: San Diego, CA

Position Description:

The Senior Administrative Services Manager (IRB Administrator) provides leadership and oversight for the Institutional Review Board (IRB) at the Naval Health Research Center (NHRC). This role is responsible for managing IRB submissions, ensuring regulatory compliance, maintaining documentation, and supporting audits in accordance with DoD, Navy, and federal regulations. The position also serves as a resource for junior staff and acts as a key liaison across research and clinical teams.


Requirements

Educational Requirements:
  • A minimum of a Bachelor's Degree in life sciences, public health, psychology, or a related field.  
Additional Qualifications:
  • A minimum of 5 years of Institutional Review Board (IRB) review experience or equivalent experience in military medical R&D activities.  
  • Certified IRB Professional (CIP) certification preferred; 2 years of relevant experience can be submitted in lieu of CIP certification.  
  • A minimum of 3 years of experience reviewing and/or managing research and development (R&D) studies.  
  • Strong knowledge of medical terminology, clinical research processes, and IRB submission/filing guidelines.  
  • Ability to communicate effectively, both orally and in writing, with diverse stakeholders including research staff, clinical teams, and senior leadership.  
  • Demonstrated organizational, analytical, and supervisory skills to manage multiple projects, staff, and regulatory requirements.  
  • Proficiency with Windows-based computer systems, including Microsoft Office Suite.  
  • Experience with government contracting or completion of a background investigation is preferred.  
  • Ability to train and mentor junior staff on IRB procedures, compliance, and regulatory best practices.  

Venesco Statement:  At Venesco, we are committed to excellence in supporting human subjects research. This role provides the opportunity to lead IRB operations, ensure regulatory compliance, and support mission-critical research initiatives while mentoring and developing junior staff in a collaborative, professional environment. 

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