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Irb Analyst Jobs in Tennessee (NOW HIRING)

Vanderbilt Health

Research Assistant 1

Nashville, TN · On-site

$18.50 - $25.50/hr

... IRB documents, consents, and clinical data) organized -Analyzing research data in collaboration with biostatisticians -Refining and enforcing team data management guidelines and data QA -Developing ...

Varsity Tutors

AP Research Tutor

Knoxville, TN · Remote

$18 - $40/hr

... analysis, academic writing conventions, and oral presentation techniques. Ability to explain ... IRB ethical requirements, and integrating multiple sources into a cohesive literature review.

Varsity Tutors

AP Research Tutor

Chattanooga, TN · Remote

$18 - $40/hr

... analysis, academic writing conventions, and oral presentation techniques. Ability to explain ... IRB ethical requirements, and integrating multiple sources into a cohesive literature review.

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Irb Analyst information

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$66.5K

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How much do irb analyst jobs pay per year?

As of Aug 29, 2026, the average yearly pay for irb analyst in Tennessee is $66,493.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,600.00 and $79,000.00 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 Tennessee?

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

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

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

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Irb Analyst jobs near you
Infographic showing various Irb Analyst job openings in Tennessee as of August 2026, with employment types broken down into 87% Full Time, 7% Part Time, and 6% Contract. Highlights an 79% Physical, 9% Hybrid, and 12% Remote job distribution, with an average salary of $66,493 per year, or $32 per hour.

Research Study Coordinator 1-Research Center (Knoxville)

The University of Tennessee

Knoxville, TN • On-site

$21.69/hr

Full-time

Posted 26 days ago

Job description


Market Range: 08
Hiring Salary: $21.69/Hourly
THIS POSITION IS LOCATED IN KNOXVILLE, TN.
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Study Coordinator 1 performs Investigator-Initiated Research for Maternal Fetal Medicine, Neonatology, and High-risk Obstetrics. This position assists the faculty with clinical research study activities including but not limited to the development, submission and management of regulatory paperwork, the submission of Institutional Review Board (IRB) applications and annual renewals, and preparation and maintenance of study files and essential trial documents
Responsibilities
  1. Assists investigators with the design of Maternal Fetal Medicine, Neonatology, and High-risk Obstetrics related studies by reviewing and/or writing proposals using methods best suited to study objectives.
  2. Assists investigators with the development and submission process for Institutional Review Board (IRB) approval including the collection of hospital collaboration agreements, key personnel documents, department approvals, funding source information, IRB application completion, and uploads in iMedRIS.
  3. Coordinates operational components of retrospective research and survey-driven research for study-specific Investigator-Initiated research for Maternal Fetal Medicine, Neonatology, and High-risk Obstetrics.
  4. Provides essential information to the GSM OB/GYN data coordinator, Physical Activity and Metabolism lab manager, or the Principal Investigator during the data analysis phase of Investigator-Initiated research.
  5. Assists investigator with the IRB process for protocol amendments and/or adding or removing IRB approved personnel from an Investigation-Initiated Project; assists faculty with the IRB process for the IRB Adverse Events, Serious Adverse Events, and Protocol Deviations.
  6. Assists in screening potential subjects, reviewing and documenting patient medical histories and concurrent medication, obtaining informed consent, coordinating study visits and procedures to be completed on campus, collecting study data, and performing study assessments if needed (lab draws, questionnaires, vital signs, etc.) for Investigator-Initiated Studies.
  7. Establishes and maintains contact with study participants and families, community agencies, and health care providers.
  8. Assists investigator with the management and maintenance of study-specific Master Study Files and Essential Study Documents.
  9. Assists with the management and maintenance of Subject Source Documents.
  10. Facilitates study-specific communication and meetings.
  11. Performs other duties as assigned.

Qualifications
EDUCATION: Bachelor's Degree in relevant health field. (TRANSCRIPT REQUIRED)
EXPERIENCE: One (1) year of relevant experience OR Associate's Degree and three (3) years of relevant experience, OR an equivalent combination of education, training, and experience to equal five (5) years.
KNOWLEDGE, SKILLS, AND ABILITIES:
  • Ability to create and maintain extensive medical records on clinical research subjects.
  • Understanding of hospital policies and procedures, medical records and documentation, and HIPAA regulations.
  • Knowledge of research protocol with an understanding of Basic Research Principles and the Federal Code of Regulations for Clinical Research Studies.
  • Ability to manage multiple priorities.
  • Ability to interact with a diverse population.
  • Intermediate-level computer skills with the ability to learn new software applications for various electronic data capture programs.
  • Ability to exhibit strong interpersonal and communication skills.

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