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Full Time Irb Analyst Jobs (NOW HIRING)

May serve as an official member of the Institutional Review Board (IRB) Committee and/or a ... Full time Shift Day (United States of America) Weekly Scheduled Hours 40 Hours of Work 9:00 a.m ...

IRB Operations Manager

Princeton, NJ ยท On-site

$130K - $170K/yr

Lead day-to-day operations of the HSPP, supervising three full-time staff while ensuring regulatory ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...

Lead day-to-day operations of the HSPP, supervising three full-time staff while ensuring regulatory ... Strong organizational, analytical, and communication skills. * Experience supporting academic ...

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time ... This position requires knowledge of IRB policies and procedures, and Federal Regulations for ...

The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time ... This position requires knowledge of IRB policies and procedures, and Federal Regulations for ...

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Full Time Irb Analyst information

See salary details

$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:

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.

IRB Analyst

Spectrum Health

Grand Rapids, MI โ€ข Hybrid

Full-time

Medical, Vision, Retirement

Posted 19 days ago


Key responsibilities

  • Assist and guide investigators through the application submission process, interpreting and advising on policies, regulations, and compliance requirements.

  • Ensure timely processing, review, and disposition of research applications in accordance with SOPs and expectations.

  • Maintain the security and integrity of regulatory data, ensuring comprehensive and compliant IRB documentation and records.


Job description

Job Summary

Responsible for all activities in support of the Human Research Protection Program (HRPP) by facilitating and participating in the regulatory review of human subject's research conducted under the jurisdiction of the Corewell Health HRPP. Provides regulatory support and oversight for the Research Community and serves as a point of contact for submission inquiries and requests for guidance and consultation as it pertains to the federal regulations, state and local laws, as well as Corewell Health Policies governing human subjects research. Ensures that Corewell Health's human research activities are conducted in compliance with institutional standard operating procedures (SOPs) and international, federal, state, and local rules and regulations and ethical principles regarding human subject research. May serve as an official member of the Institutional Review Board (IRB) Committee and/or a "designated" reviewer, as applicable.

Essential Functions
  • Assists and guides investigators through the application submission process. Interprets and advises investigators on applicable policies, procedures, guidelines, federal regulations, and other compliance related requirements. Functions as a liaison within and between the IRB committee, investigators and their designees, and other research support staff.
  • Ensures timely processing, review and disposition of research applications within established expectations and SOPs.
  • Serves as an official member of the IRB Committee and/or a "designated" reviewer, as applicable.
  • Serves as the lead for the assigned team and provides guidance and mentorship across the department regarding complex HRPP issues/situations.
  • Responsible for maintaining the security and integrity of federally and contractually mandated regulatory data assuring comprehensive and compliant IRB documentation and records in accordance with regulations and SOPs. Responsible for the maintenance and retention of all required IRB records, communications and other files for assigned submissions.
  • Possesses a comprehensive and broad understanding and knowledge of federal and state regulations, state and local law and IRB SOPs. Develops SOPs and policies for the HRPP to include topics such as IRB Operations, Overarching special topic guidance sheets, HIPAA in relation to research and Conflicts of Interest in research.
  • Assists with the conduct of HRPP Post Approval Monitoring activities as required by federal regulations and local SOPs. Develops and implements effective HRPP educational strategies.
Qualifications

Required

  • Bachelor's degree or equivalent preferred areas of study include clinical, life or social sciences

Preferred

  • Master's Degree
  • 2 years of relevant experience IRB administration, clinical research or other human subject protection-related job or other analytical or compliance
  • Direct and obvious relevance to regulatory compliance and/or research with human subjects
  • Relevant program/project management experience
  • CRT-IRB Professional, Certified (CIP)

About Corewell Health

As a team member at Corewell Health, you will play an essential role in delivering personalized health care to our patients, members and our communities. We are committed to cultivating and investing in YOU. Our top-notch teams are comprised of collaborators, leaders and innovators that continue to build on one shared mission statement - to improve health, instill humanity and inspire hope. Join a nationally recognized health system with an ambitious vision of continued advancement and excellence.


How Corewell Health cares for you
  • Comprehensive benefits package to meet your financial, health, and work/life balance goals. Learn more here.
  • On-demand pay program powered by Payactiv
  • Discounts directory with deals on the things that matter to you, like restaurants, phone plans, spas, and more!
  • Optional identity theft protection, home and auto insurance
  • Traditional and Roth retirement options with service contribution and match savings
  • Eligibility for benefits is determined by employment type and status

Primary Location

SITE - Secchia Center - 15 Michigan St NE - Grand Rapids

Department Name

Sponsored Programs Instiutional Review Board - Grand Rapids Hosp

Employment Type

Full time

Shift

Day (United States of America)

Weekly Scheduled Hours

40

Hours of Work

9:00 a.m. - 5:00 p.m.

Days Worked

Monday to Friday

Weekend Frequency

N/A

CURRENT COREWELL HEALTH TEAM MEMBERS - Please apply through Find Jobs from your Workday team member account. This career site is for Non-Corewell Health team members only.

Corewell Health is committed to providing a safe environment for our team members, patients, visitors, and community. We require a drug-free workplace and require team members to comply with the MMR, Varicella, Tdap, and Influenza vaccine requirement if in an on-site or hybrid workplace category. We are committed to supporting prospective team members who require reasonable accommodations to participate in the job application process, to perform the essential functions of a job, or to enjoy equal benefits and privileges of employment due to a disability, pregnancy, or sincerely held religious belief.

Corewell Health grants equal employment opportunity to all qualified persons without regard to race, color, national origin, sex, disability, age, religion, genetic information, marital status, height, weight, gender, pregnancy, sexual orientation, gender identity or expression, veteran status, or any other legally protected category.

An interconnected, collaborative culture where all are encouraged to bring their whole selves to work, is vital to the health of our organization. As a health system, we advocate for equity as we care for our patients, our communities, and each other. From workshops that develop cultural intelligence, to our inclusion resource groups for people to find community and empowerment at work, we are dedicated to ongoing resources that advance our values of diversity, equity, and inclusion in all that we do. We invite those that share in our commitment to join our team.

You may request assistance in completing the application process by calling 616.486.7447.