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Full Time Irb Analyst Jobs (NOW HIRING)

TCS Education System

Research Compliance Specialist

Chicago, IL · On-site +1

$68K - $70K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

... 600 full-time faculty and staff. As an institution, The Chicago School is deeply committed to ... Conduct for-cause audits authorized by the IRB or institutional official. * Conduct periodic ...

University of Utah

PS Regulatory Coordinator

Campus, IL · On-site

  • Retirement

Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Coordinates with study sponsor, investigator and IRB to complete study closure activities.

University of Utah

PS Regulatory Coordinator

Campus, IL · On-site

  • Retirement

Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary VP ... Coordinates with study sponsor, investigator and IRB to complete study closure activities.

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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 Aug 14, 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 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 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 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.

How to become a full time IRB analyst?

To become a full-time IRB analyst, candidates typically need a bachelor's degree in a related field such as healthcare, biology, or ethics, along with experience in research compliance or regulatory environments. Certification from organizations like the Certified IRB Professional (CIP) can enhance job prospects, and strong attention to detail, knowledge of federal regulations, and proficiency with research protocols are essential. Most positions require familiarity with IRB review processes and ethical standards in research.

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.
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What states have the most Full Time Irb Analyst jobs?

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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 1% Internship, 86% Full Time, 6% Part Time, and 7% Contract. Highlights an 81% Physical, 9% Hybrid, and 10% Remote job distribution, with an average salary of $88,569 per year, or $42.6 per hour.

Clinical Research Coordinator

New York Medical College

Hawthorne, NY • On-site

$43K - $54K/yr

Full-time

Re-posted 2 days ago

Job description

Overview
The Division of Medical Genetics at New York Medical College is seeking a clinical research coordinator to work with our team on multiple clinical trials. The ideal candidate has 2 years of clinical trial experience, but we are willing to train the right candidate. The coordinator will be working on investigational drug studies as well as prospective and retrospective data entry for multiple studies.
Category: Full-time, Grant Supported Position-(Position is contingent on continued funding)
Responsibilities
• Review and analysis of clinical trial protocols and informed consent forms
• Assist Principal and Sub-Investigator in study start-up process
• Coordinate budget review and IRB reviews
• Submission of regulatory documents and communication with IRB
• Data entry, management of queries
• Managing supply of investigational study drug with temperature monitoring
• Invoicing Study Sponsor for study procedures as per contract requirements.
• Coordinating transportation and lodging (as needed) with submission of patient travel and meal receipts to Sponsor
• Management of medical supplies and related product orders
• Packing and shipping of clinical laboratory specimens
• Maintain source documents in accordance with FDA and GCP guidelines
• Other duties as assigned
Qualifications
  • Bachelor's degree required, preferably in health-science field
  • Proficiency with Microsoft Office suite, including Word, Excel, and Outlook
  • Must be adept at keeping track of multiple projects, able to work independently, and have strong problem solving, communication, and analytical skills

Minimum Salary
USD $43,680.00/Yr.
Maximum Salary
USD $54,600.00/Yr.

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