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Irb Jobs in Florida (NOW HIRING)

BayCare Health System

IRB Coordinator

Clearwater, FL · On-site

IRB Coordinator Facility: BayCare Systems Office (Clearwater, FL) Schedule: Tuesday - Thursday in office, Monday & Friday work from home Responsibilities: * Provide functional support to the ...

BayCare Health System

IRB Coordinator

Clearwater, FL · On-site

IRB Coordinator Facility: BayCare Systems Office (Clearwater, FL) Schedule: Tuesday - Thursday in office, Monday & Friday work from home Responsibilities: * Provide functional support to the ...

K2 Staffing LLC

Regulatory Associate

Lady Lake, FL · On-site

Prepare regulatory documents for new study submissions to IRB and sponsor * Maintain regulatory files at audit-ready status at all times by ensuring filing are up-to-date upon completion of the ...

K2 Staffing LLC

Regulatory Associate

Tampa, FL · On-site

Prepare regulatory documents for new study submissions to IRB and sponsor * Maintain regulatory files at audit-ready status at all times by ensuring filing are up-to-date upon completion of the ...

Evolution Research Group

Sub l /Nurse Practitioner

Miami, FL · On-site

$98K - $133K/yr

Provide the sponsor and IRB with documentation of credentials as requested. * Demonstrate the proper education, training, and experience to conduct the clinical investigation. * Assume responsibility ...

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How much do irb jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for irb in Florida is $30.61, according to ZipRecruiter salary data. Most workers in this role earn between $19.15 and $39.83 per hour, depending on experience, location, and employer.

What is an IRB?

An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects. The primary purpose of the IRB is to ensure that the rights, welfare, and privacy of participants are protected throughout the research process. IRBs review research proposals to ensure ethical standards are met and that risks to participants are minimized. They are required for most research conducted at universities, hospitals, and other organizations that receive federal funding.

What are the typical responsibilities of an IRB coordinator, and how do they interact with researchers and regulatory bodies?

An IRB (Institutional Review Board) coordinator is responsible for managing the review process of research protocols involving human subjects to ensure compliance with ethical standards and federal regulations. This role involves working closely with researchers to guide them through the submission process, reviewing applications for completeness, and facilitating communication between the IRB committee and research teams. Coordinators also serve as liaisons with regulatory bodies, maintain records, and help organize IRB meetings. Strong organizational, communication, and regulatory knowledge are essential, as coordinators often balance multiple projects and deadlines while ensuring research integrity and participant safety.

What are the key skills and qualifications needed to thrive as an IRB administrator, and why are they important?

To thrive as an IRB Administrator, you need expertise in research ethics, regulatory compliance, and human subject protection, usually supported by a relevant bachelor's or master's degree. Familiarity with IRB management software, federal regulations (such as the Common Rule), and certifications like CIP (Certified IRB Professional) are typically required. Strong organizational skills, attention to detail, and effective communication are crucial for coordinating reviews and guiding researchers. These skills ensure ethical research practices, regulatory compliance, and the protection of research participants.

What is the difference between Irb vs Clinical Research Coordinator?

AspectIrbClinical Research Coordinator
Required CredentialsOften requires IRB training, ethics certificationRequires research experience, sometimes certifications
Work EnvironmentReview boards, research institutionsClinical sites, hospitals, research centers
Employer & Industry UsageUsed in research oversight, ethics reviewUsed in managing clinical trials, patient coordination
Common Search & Comparison IntentUnderstanding roles in research ethicsUnderstanding clinical trial management

IRBs (Institutional Review Boards) focus on ethical review and approval of research protocols, ensuring participant safety. Clinical Research Coordinators manage the day-to-day operations of clinical trials, including patient recruitment and data collection. While both roles are integral to clinical research, IRBs oversee ethical compliance, whereas Coordinators handle trial execution.

How to get an IRB job?

To get an IRB (Institutional Review Board) job, candidates typically need a background in research ethics, healthcare, or related fields, along with relevant experience. Certifications such as the CITI Program Human Subjects Research course are often required, and strong knowledge of federal regulations like 45 CFR 46 is beneficial. Positions may involve reviewing research protocols to ensure ethical standards are met and often require attention to detail and good communication skills.

What does an IRB analyst do?

An IRB analyst reviews research protocols to ensure they comply with ethical standards and regulatory requirements. They evaluate risks, consent processes, and study procedures, often working with institutional review boards to approve or modify research proposals. Strong attention to detail and knowledge of federal regulations are essential for this role.

What are the most commonly searched types of Irb jobs in Florida?

The most popular types of Irb jobs in Florida are:

What are popular job titles related to Irb jobs in Florida?

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

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

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What cities in Florida are hiring for Irb jobs?

Cities in Florida with the most Irb job openings:

Irb jobs near you
Infographic showing various Irb job openings in Florida as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $63,665 per year, or $30.6 per hour.

IRB Coordinator

BayCare Health System

Clearwater, FL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 25 days ago

BayCare Health System rating

7.5

Company rating: 7.5 out of 10

Based on 403 frontline employees who took The Breakroom Quiz

236th of 889 rated healthcare providers

Job description

Join the team that is revolutionizing health care - BayCare Health System
Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that's built on a foundation of trust, dignity, respect, responsibility, and clinical excellence.
Title: IRB Coordinator
Facility: BayCare Systems Office (Clearwater, FL)
Schedule: Tuesday - Thursday in office, Monday & Friday work from home
Responsibilities:
  • Provide functional support to the Institutional Review Board (IRB).
  • Responsible for certain administrative aspects of IRB support, including preparation of IRB agenda and minutes, processing of IRB applications, maintenance of IRB files, preparation of IRB approval letters, initial application support, and pre-review activities.
  • Perform other duties as assigned.

BayCare offers a competitive total reward package including:
  • Benefits (Medical, Dental, Vision)
  • Paid Time Off
  • Tuition Assistance
  • 401K Match and additional yearly contribution
  • Annual performance appraisals and team award bonus
  • Family resources and wellness opportunities
  • Community perks and discounts

Required Experience & Education:
  • Required - Associates Degree in Science and 2 years IRB, Research, or Healthcare experience
  • Or - Bachelor's Degree in Healthcare of related field and 1 year Research experience
  • Research experience is strongly preferred

Location: Clearwater, FL
Status: Full Time, Exempt: No
Shift Hours: 8:00AM - 4:30PM
Weekend Work: None
Equal Opportunity Employer Veterans/Disabled

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