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Irb Analyst Jobs in Virginia (NOW HIRING)

Integral

Compliance and Risk Analyst

Tysons Corner, VA · On-site

$100K - $120K/yr

... IRB) process, and others. * Maintain an IT Investment Portfolio in support of IT technology ... Options analysis to include modification of existing technology vs. replacement * Metrics to be ...

Integral

Compliance and Risk Analyst

Tysons, VA · On-site

$100K - $120K/yr

... IRB) process, and others. * Maintain an IT Investment Portfolio in support of IT technology ... Options analysis to include modification of existing technology vs. replacement * Metrics to be ...

Prism Vision Group

Clinical Research Assistant

Fairfax, VA · On-site

$46K - $96K/yr

... analysis of clinical research data. The Clinical Research Assistant will develop knowledge of the ... Responsible for submissions and reports to the IRB; maintains documentation of IRB communications ...

New

GAP SOLUTIONS INC

... IRB, biosafety, and federal regulatory requirements, thereby enabling timely research analysis, participant safety reporting, and successful execution of NIAID clinical research activities. This role ...

Prism Vision Group

Clinical Research Assistant

Fairfax, VA

$46K - $96K/yr

... analysis of clinical research data. The Clinical Research Assistant will develop knowledge of the ... Responsible for submissions and reports to the IRB; maintains documentation of IRB communications ...

Posted today

MEI Rigging & Crating

Safety Manager

Chantilly, VA · On-site

Work collectively with Incident Review Board (IRB) and Site management to manage all incidents and accident cases thru investigations and root cause analysis, including working directly with ...

BLN24

Social Science Research Lead

Mclean, VA · On-site

$90 - $120/hr

... analyses, literature reviews, research syntheses, and program evaluations that identify emerging ... Support compliance activities related to Institutional Review Boards (IRB), Paperwork Reduction Act ...

BLN24

Social Science Research Lead

Mclean, VA · On-site

... analyses, literature reviews, research syntheses, and program evaluations that identify emerging ... Support compliance activities related to Institutional Review Boards (IRB), Paperwork Reduction Act ...

Virginia Heart

Clinical Research Coordinator

Leesburg, VA

$24.50 - $32.50/hr

Strong organizational and analytical skills required * In depth knowledge of Good Clinical Practice (GCP), FDA regulations, and IRB requirements * Proficiency and clinical trial management systems ...

Direct Jobs

Research Manager - Cancer Analytics

Fairfax, VA · On-site

$110 - $150/hr

Demonstrable knowledge or experience with IRB processes, data governance, and/or clinical data analytics or operations (oncology preferred) in a healthcare setting. * Familiarity with Epic, research ...

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Irb Analyst information

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$30.7K

$72.6K

$128.9K

How much do irb analyst jobs pay per year?

As of Aug 14, 2026, the average yearly pay for irb analyst in Virginia is $72,633.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,000.00 and $86,300.00 per year, depending on experience, location, and employer.

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 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. The role requires attention to detail, knowledge of federal regulations, and effective communication with researchers.

How to become an IRB analyst?

To become an IRB analyst, typically a bachelor's degree in health sciences, research, or a related field is required. Relevant skills include knowledge of research ethics, regulatory compliance, and experience with institutional review board processes; certifications such as CITI training can also be beneficial.

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 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. Strong knowledge of federal regulations, good communication skills, and attention to detail are essential, and some roles may require certification such as the Certified IRB Professional (CIP).

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 most commonly searched types of Irb Analyst jobs in Virginia?

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

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

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Irb Analyst jobs near you
Infographic showing various Irb Analyst job openings in Virginia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 74% In-person, and 26% Remote job distribution, with an average salary of $72,633 per year, or $34.9 per hour.

Human Research Protection Program Analyst

Hyperion Biotechnology, Inc.

Falls Church, VA

Full-time

Posted 15 days ago

Job description

Human Research Protection Analyst Summary

The Human Research Protection Analyst supports the Human Research Protection Program (HRPP) by ensuring compliance with federal regulations, ethical standards, and institutional policies governing human subjects research. This position provides regulatory guidance, conducts compliance reviews and site inspections, supports Institutional Review Boards (IRBs), and serves as a subject matter expert on human research protections.

Job Duties

  • Conducts compliance review of IRB minutes and protocol submissions to monitor compliance with Federal, Department of War (DoW), and Navy human subjects research requirements.
  • Serves as point-of-contact for assigned commands and provides guidance, training, and oversight, as needed.
  • Serves as a subject matter expert to HRPP staff, IRB members, Human Research Protections Officials (HRPOs), and others, as needed, on human subjects research regulations, policies, and procedures. Subject matter expertise must include knowledge of applicable Federal, DoW, Navy, and Food and Drug Administration (FDA) regulations, requirements, and standards.
  • Conducts site assessments and assist visits with Navy commands research sites on a regular basis.
  • Coordinates with the command HRPP staff and other site assessment or assist visit team members, including leadership. Site assessments and assist visits may include interviews with human research protection staff, interviews with researchers, review of command HRPP files, and review of investigator files.
  • Evaluates and assess visit findings objectively and integrates all activities and results into a final assessment report or summary.
  • Serves as a site assessment or assist visit team member for other DON HRPP visits, as needed.
  • Assists in the development and implementation of human subject protection standards, policies, procedures and systems relative to medical research and cross-discipline human subjects research, research subject protection, and institutional and investigator compliance.
  • Periodically reviews command assurances for the protection of human subjects. Assurance reviews can include an application, command instructions, IRB roster, HRPP Policies and Procedures, agreements, and other documents.
  • Reviews and analyzes institution-specific HRPP instructions, policies, and procedures. Provides feedback including specific findings and recommendations to further institutional compliance and/or initiate quality improvements, as needed.
  • Interprets results of compliance reviews and analysis to determine significant trends, and prepares and presents reports, interpretations, conclusions, and impacts of these trends.
  • Identifies need for new processes, systems, methods or approaches, guidance documents, standards, and training needs for the supported HRPPs.
  • Provides consultation for updating regulations and policies, as needed.
  • Produces high-quality graphs using Excel, specialized analytics software, and leveraging artificial intelligence (AI) resources, as appropriate.

Job Requirements

Bachelor's degree in biomedical or socio-behavioral field required. Masters preferred.

Minimum of 4 years' experience in human research protections and compliance oversight, including experience supporting an IRB.

Exceptional communication skills (verbal and written), with proven technical writing abilities (Writing sample required to be provided).

Proficiency in data analytics and visualization tools (such as Excel, Power BI, Tableau) including AI utilities, to generate executive-ready data displays and reports.

Travel: Domestic and International required up to 4 times per year. Passport Required.

Human research protections or regulatory compliance certification (or obtained within 6 months of hire) is preferred.

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