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Full Time Irb Analyst Jobs (NOW HIRING)

May Institute

Behavior Analyst (BCBA)

Randolph, MA · On-site

$77K - $87K/yr

Behavior Analyst I (BCBA) - Randolph MA ABA Center $5,000 SIGN-ON Bonus! Full-Time | Randolph, MA ... Access to our own Institutional Review Board (IRB) to support research and publication.

mayinstitute

Behavior Analyst (BCBA)

Randolph, MA · On-site

$77K - $87K/yr

Behavior Analyst I (BCBA) - Randolph MA ABA Center $5,000 SIGN-ON Bonus! Full-Time | Randolph, MA ... Access to our own Institutional Review Board (IRB) to support research and publication.

Tilda Research

... like IRB interactions, Study Protocols, Delegation of Authority, inventory logs, etc. We will ... Employment Type: FULL_TIME

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Full Time Irb Analyst information

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$49K

$88.6K

$123.5K

How much do full time irb analyst jobs pay per year?

As of Sep 7, 2026, the average yearly pay for full time irb analyst in the United States is $88,569.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,000.00 and $99,500.00 per year, depending on experience, location, and employer.

What is a full time IRB analyst?

Full Time IRB Analysts are professionals who review research proposals to ensure they comply with ethical standards and federal regulations for human subject research. They work within Institutional Review Boards (IRBs) at universities, hospitals, or research organizations. Their responsibilities include evaluating study protocols, ensuring informed consent, and safeguarding participants' rights and welfare. Full time analysts typically collaborate with researchers and provide guidance on regulatory requirements. This role requires strong attention to detail and knowledge of ethical research practices.

What are the key skills and qualifications needed to thrive as a full time IRB analyst?

To thrive as a Full Time IRB Analyst, you need a solid understanding of research ethics, regulatory compliance, and human subjects protection, often supported by a relevant degree in health sciences or a related field. Familiarity with electronic IRB management systems, federal regulations (like the Common Rule), and certifications such as CIP (Certified IRB Professional) are typically required. Strong analytical thinking, attention to detail, and effective communication skills help you interpret protocols and interact with researchers and committee members. These skills are crucial to ensure ethical research practices, regulatory compliance, and the protection of participants' rights and welfare.

What are some common challenges faced by full time IRB analysts, and how can they be managed effectively?

Full Time IRB Analysts often encounter challenges related to balancing regulatory compliance with facilitating research efficiency. Navigating complex federal regulations, staying updated on policy changes, and managing high volumes of protocol submissions can be demanding. Effective time management, strong communication skills for liaising with researchers and committee members, and continuous professional development are key to managing these challenges. Collaborative team environments and mentorship opportunities also help IRB Analysts stay informed and support each other.

What is the difference between Full Time Irb Analyst vs Part Time Irb Analyst?

AspectFull Time Irb AnalystPart Time Irb Analyst
Work HoursTypically 40 hours/weekLess than 20 hours/week
CertificationsOften requires IRB-related certificationsMay require similar certifications but on a part-time basis
Work EnvironmentFull-time, office or remotePart-time, flexible schedule
Employer UsageCommon in research institutions and biotech companiesLess common, often in consulting or freelance roles

Full Time Irb Analysts typically work 40 hours a week, with comprehensive responsibilities in overseeing research compliance. Part Time Irb Analysts work fewer hours, often with flexible schedules, focusing on specific tasks. Both roles require similar certifications and are used in research settings, but full-time positions offer more stability and broader responsibilities.

More about Full Time Irb Analyst jobs

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

The most popular types of Irb Analyst jobs are:

What states have the most Full Time Irb Analyst jobs?

States with the most job openings for Full Time Irb Analyst jobs include:

What job categories do people searching Full Time Irb Analyst jobs look for?

The top searched job categories for Full Time Irb Analyst jobs are:

Full Time Irb Analyst jobs near you
Infographic showing various Full Time Irb Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 6% Part Time, and 5% Contract. Highlights an 82% Physical, 7% Hybrid, and 11% Remote job distribution, with an average salary of $88,569 per year, or $42.6 per hour.

Regulatory Analyst, Human Research Protection

UT Southwestern Medical Center

Dallas, TX • On-site

Full-time

Medical, Retirement, 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

111th 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. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you'll discover a culture of teamwork, professionalism, and a rewarding career!
JOB SUMMARY
The purpose of this job is to work closely with investigators and research personnel on the development and refinement of proposals for the performance of human clinical trials or animal research. 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.
BENEFITS
UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include:
  • PPO medical plan, available day one at no cost for full-time employee-only coverage
  • 100% coverage for preventive healthcare-no copay
  • Paid Time Off, available day one
  • Retirement Programs through the Teacher Retirement System of Texas (TRS)
  • Paid Parental Leave Benefit
  • Wellness programs
  • Tuition Reimbursement
  • Public Service Loan Forgiveness (PSLF) Qualified Employer
  • Learn more about these and other UTSW employee benefits!

EXPERIENCE AND EDUCATION
Required
  • Education
    Bachelor's Degree in related field or
    Master's Degree in related field
  • Experience
    3 years related experience with Bachelor's degree. or
    1 year related experience with Master's degree.
Preferred
  • Education
    Advanced science degree and extensive current knowledge of regulations governing human or animal research protections strongly preferred.
  • Experience
    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.
SECURITY AND EEO STATEMENT
Security
This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information.
EEO
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.

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