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Irb Manager Jobs in Florida (NOW HIRING)

Careerxchange

Sr Clinical Research Coordinator

Miami, FL · On-site

$32 - $43/hr

... and IRB processes. * Excellent organizational, communication, and multitasking skills. * Proficiency with electronic medical records (EMR) and clinical trial management systems is preferred.

University of Miami

Regulatory Analyst 2

Miami, FL · On-site

$70 - $95/hr

This position requires knowledge of IRB policies and procedures, and Federal Regulations for ... Provides updates to the study team and/or management regarding submission statutes and approvals (e ...

The University of Miami

Regulatory Analyst 2

Miami, FL · On-site

This position requires knowledge of IRB policies and procedures, and Federal Regulations for ... Provides updates to the study team and/or management regarding submission statutes and approvals (e ...

University of Miami

Regulatory Analyst 2

Miami, FL · On-site

This position requires knowledge of IRB policies and procedures, and Federal Regulations for ... Provides updates to the study team and/or management regarding submission statutes and approvals (e ...

UAB

CLINICAL RESEARCH NURSE COORDINATOR I

Tampa, FL

$52K - $85K/yr

Coordinates and manages clinical care activities for pediatric hematology/oncology patients ... Ensures compliance with federal regulations, IRB requirements, sponsor guidelines, and Good ...

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Irb Manager information

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$43.7K

$58.7K

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How much do irb manager jobs pay per year?

As of Sep 4, 2026, the average yearly pay for irb manager in Florida is $58,730.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,000.00 and $60,900.00 per year, depending on experience, location, and employer.

What is an IRB manager?

An IRB (Institutional Review Board) Manager oversees the ethical review process for research involving human subjects, ensuring compliance with federal regulations and institutional policies. They coordinate IRB meetings, review study protocols, and assist researchers in navigating the approval process. The role involves training staff, maintaining records, and staying updated on regulatory changes to protect human research participants.

What are the key skills and qualifications needed to thrive as an IRB manager?

To thrive as an IRB Manager, you need expertise in research ethics, regulatory compliance, and protocol review, often supported by a bachelor’s or master’s degree in a related field and experience with Institutional Review Boards. Familiarity with electronic IRB management systems (such as IRBNet or iMedRIS) and professional certifications like CIP (Certified IRB Professional) are also beneficial. Strong organizational skills, attention to detail, and effective communication help facilitate collaboration with researchers and regulatory bodies. These competencies ensure ethical research practices and efficient, compliant review processes within institutions.

What are some common challenges faced by IRB managers in their daily work?

IRB Managers frequently navigate the complex and evolving landscape of federal, state, and institutional regulations governing human subjects research, which can be both challenging and rewarding. They must balance thorough protocol reviews with timely decision-making, ensuring research projects start on schedule while safeguarding participant welfare. Managing communication between researchers, IRB members, and compliance officers requires strong organizational skills and diplomacy. These challenges make the role dynamic and integral to maintaining the integrity of research within the institution.

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 Manager jobs in Florida?

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

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

The top searched job categories for Irb Manager jobs in Florida are:

What cities in Florida are hiring for Irb Manager jobs?

Cities in Florida with the most Irb Manager job openings:

Irb Manager jobs near you
Infographic showing various Irb Manager job openings in Florida as of August 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $58,730 per year, or $28.2 per hour.

Sr Clinical Research Coordinator

Careerxchange

Miami, FL • On-site

$32 - $43/hr

Contractor

Re-posted 24 days ago

Job description

Location: Miami, FL
Job Type: Contract (15 Weeks)
Schedule: Monday – Friday, 8:30 AM – 5:00 PM
Pay: $32.00 – $43.00 per hour


Job Summary
We are seeking an experienced Senior Clinical Research Coordinator to support a busy clinical research team during a 15-week contract assignment. This role is responsible for coordinating all aspects of clinical research studies, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines while delivering exceptional patient care.


Responsibilities
  • Coordinate and manage multiple clinical research studies from start-up through closeout.
  • Screen, recruit, consent, and schedule study participants.
  • Collect, document, and maintain accurate study data and source documentation.
  • Ensure compliance with FDA, IRB, GCP, and sponsor requirements.
  • Prepare for sponsor visits, monitoring visits, and audits.
  • Coordinate study procedures, laboratory specimens, and investigational product accountability.
  • Maintain regulatory binders and study documentation.
  • Communicate effectively with investigators, sponsors, research staff, and participants.
  • Assist with data entry, query resolution, and timely reporting of adverse events.

Qualifications
  • 3+ years of clinical research coordination experience required.
  • Experience coordinating industry-sponsored clinical trials.
  • Strong knowledge of GCP, FDA regulations, and IRB processes.
  • Excellent organizational, communication, and multitasking skills.
  • Proficiency with electronic medical records (EMR) and clinical trial management systems is preferred.
  • Current CPR certification and Clinical Research certification (CCRC or CCRP) are a plus.


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