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Irb Analyst Jobs in Texas (NOW HIRING)

Senior Data Analyst

Dallas, TX · On-site

$85K - $107K/yr

This position will also participate in the analysis of research data for the Trauma Research ... Lead evaluation projects including design, data collection, and IRB applications * Oversee and ...

... IRB processes, grant administration, and research compliance - Experience with data analysis, health informatics, or mixed-methods research preferred - Excellent communication skills and ability to ...

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Irb Analyst information

See Texas salary details

$28.9K

$68.3K

$121.1K

How much do irb analyst jobs pay per year?

As of Sep 3, 2026, the average yearly pay for irb analyst in Texas is $68,254.00, according to ZipRecruiter salary data. Most workers in this role earn between $48,900.00 and $81,100.00 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 Texas?

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

What job categories do people searching Irb Analyst jobs in Texas look for?

The top searched job categories for Irb Analyst jobs in Texas are:

What cities in Texas are hiring for Irb Analyst jobs?

Cities in Texas with the most Irb Analyst job openings:

Infographic showing various Irb Analyst job openings in Texas as of August 2026, with employment types broken down into 86% Full Time, 7% Part Time, 6% Contract, and 1% Nights. Highlights an 79% Physical, 8% Hybrid, and 13% Remote job distribution, with an average salary of $68,254 per year, or $32.8 per hour.

Regulatory Analyst, Human Research Protection

UT Southwestern Medical Center

Dallas, TX • On-site

Full-time

Medical, PTO

Re-posted 7 days ago


UT Southwestern rating

7.9

Company rating: 7.9 out of 10

Based on 152 frontline employees who took The Breakroom Quiz

110th of 898 rated healthcare providers


Job description

Why UT Southwestern?
With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. At UT Southwestern, we invest in you with opportunities for career growth and development that align with your future goals and help to provide security for you and your family. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more that are all available on the day you start work. UT Southwestern is honored to be a Veteran Friendly work environment that is home to approximately 800 veterans. We value your integrity, dedication, and the commitment you've made to our country. We're proud to support your next mission. Ranked by Forbes as one of the Top 10 National Employers, we invite you to be a part of the UT Southwestern team where you'll discover teamwork, professionalism, and consistent opportunities for growth.
Job Summary
UT Southwestern Medical Center is hiring for Regulatory Analyst, Human Research Protection
The Regulatory Analyst will perform protocol pre-review prior to submission to the IRB. Provide consultation to PI on regulatory, scientific, or policy issues. Collaborate with IRB and other regulatory entities at the institution to provide optimal protocol review services for PIs. Directs, analyzes, coordinates, and evaluates research program operation and procedures. Develop, cultivate, and maintain working relationships with internal/external departments/agencies associated with and/or receiving benefit from the research program. Establish research program goals and objectives. Recommend new policies/procedures for improvement of program activities. Responsible for design, execution, and effectiveness of system of internal controls. Ensures compliance with applicable laws, regulations, policies, and procedures. Reads literature and attends training as necessary.
Experience and Education
  • Bachelor's degree in related field and three (3) years related experience or a Master's degree in related field and one (1) years of related experience is required.
  • Advanced science degree and extensive current knowledge of regulations governing human or animal research protections strongly preferred. Previous service on an IRB or IACUC a plus.
Job Duties
  • For campus-wide research, perform thorough protocol pre-review in advance of submission to the Institutional Review Board (IRB) or Institutional Animal Care and Use Committee (IACUC) and provide technical consultation to Principal Investigators on any regulatory, scientific, or policy issues that will affect the likelihood of IRB/IACUC approvals.
  • Collaborates closely with the IRB or IACUC and other regulatory entities at the institution to provide optimal protocol review services for investigators.
  • Directs, analyzes, coordinates, and evaluates research program operation and procedures.
  • Develops, cultivates, and maintains working relationships with internal/external departments/agencies and other organizations associated with and/or receiving benefit from the research program.
  • Establishes research program goals and objectives and directs clinical trials program evaluation and quality control activities; develops and/or approves schedules, priorities, and standards for achieving goals.
  • Recommends new policies and procedures for improvement of program activities.
  • Responsible for design, execution, and effectiveness of system of internal controls, which provide reasonable assurance that operations are effective and efficient.
  • Ensures compliance with applicable laws, regulations, policies, and procedures.
  • Reads literature and attends training and other functions as necessary to keep abreast of relevant scientific, regulatory, and technical developments related to oversight of research.
  • Performs other duties as assigned.
Knowledge, Skills & Abilities
  • Work requires excellent verbal, written, and interpersonal communication skills to work effectively with all levels of staff, faculty, and scientists.
  • Work requires ability to read, write, analyze data, develop plans and procedures, and coordinate resources to accomplish goals.
  • Work requires ability to provide technical assistance and consultation to physicians and other scientists.
  • Work requires responsibility for review, recommendation, development, and implementation of policies.
  • Work requires computer proficiency and comfort with electronic technology for data management.
Working Conditions
  • Work is performed primarily in general office area.

To learn more about the benefits UT Southwestern offers, visit https://www.utsouthwestern.edu/employees/hr-resources/
This position is security-sensitive and subject to Texas Education Code §51.215, which authorizes UT Southwestern to obtain criminal history record information. UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.
To learn more, please visit: https://jobs.utsouthwestern.edu/why-work-here/diversity-inclusion

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