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Full Time Irb Jobs in Florida (NOW HIRING)

BayCare Health System

IRB Coordinator

Clearwater, FL · On-site

Title: IRB Coordinator Facility: BayCare Systems Office (Clearwater, FL) Schedule: Tuesday ... Clearwater, FL Status: Full Time, Exempt: No Shift Hours: 8:00AM - 4:30PM Weekend Work: None Equal ...

K2 Staffing LLC

Regulatory Associate

Lady Lake, FL · On-site

Prepare regulatory documents for new study submissions to IRB and sponsor * Maintain regulatory ... Our comprehensive benefits package for full-time employees includes medical, dental, and vision ...

K2 Staffing LLC

Regulatory Associate

Tampa, FL · On-site

Prepare regulatory documents for new study submissions to IRB and sponsor * Maintain regulatory ... Our comprehensive benefits package for full-time employees includes medical, dental, and vision ...

SRA Trials

Clinical Research Coordinator

Miami, FL · On-site

$57K - $80K/yr

Correspondence with sponsors, labs, IRB, and other regulatory organizations * Maintain organized ... Bilingual- English and Spanish required Job Type: Full-time Benefits: * Dental Insurance * Health ...

University of Miami

Regulatory Analyst 2

Miami, FL · On-site

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 information

What is a full time IRB?

A Full Time IRB (Institutional Review Board) professional is a specialist who works full-time to review, approve, and oversee research involving human subjects to ensure that ethical standards and regulatory requirements are met. They are responsible for protecting the rights and welfare of research participants by conducting ethical reviews, monitoring ongoing research, and providing guidance to researchers. Full Time IRB staff often work in universities, hospitals, or research institutions, and collaborate closely with researchers and compliance officers. Their role is essential to maintaining the integrity and safety of scientific research involving humans.

What are the typical responsibilities of a full time IRB coordinator, and how does the role interact with researchers and regulatory bodies?

A full-time IRB coordinator is responsible for managing the ethical review process of research involving human subjects. This includes reviewing research proposals for compliance with federal regulations, facilitating IRB meetings, communicating required changes to researchers, and maintaining accurate records. Coordinators act as a critical liaison between researchers, IRB members, and regulatory agencies to ensure studies are conducted ethically and participants are protected. Daily tasks often involve document review, correspondence, and providing guidance to investigators, making strong communication and organizational skills essential.

What are the key skills and qualifications needed to thrive as a full time IRB professional, and why are they important?

To thrive as a full-time IRB professional, you need a comprehensive understanding of research ethics, regulatory compliance (such as 45 CFR 46 and FDA regulations), and typically a background in life sciences or healthcare. Familiarity with electronic IRB management systems, compliance databases, and certifications like CIP (Certified IRB Professional) are commonly required. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for reviewing protocols and collaborating with researchers. These competencies are critical for ensuring the protection of human research subjects and maintaining institutional and federal compliance.

What is the difference between Full Time Irb vs Part Time Irb?

AspectFull Time IrbPart Time Irb
CredentialsIRB certification, research ethics trainingIRB certification, research ethics training
Work EnvironmentOffice, research institutions, hospitalsFlexible, part-time settings, remote options
Employer & IndustryResearch institutions, hospitals, universitiesResearch organizations, academic institutions
Work Hours40+ hours/weekLess than 20 hours/week

Full Time Irb roles typically involve a standard 40+ hour workweek, requiring full-time commitment and consistent presence in research settings. Part Time Irb positions offer flexible hours, often less than 20 hours weekly, suitable for those balancing other responsibilities. Both roles require IRB certification and knowledge of research ethics, but the main difference lies in hours and work setting.

How to become a full time IRB?

To become a full-time IRB (Institutional Review Board) member, individuals typically need a background in research, ethics, or related fields, along with experience in human subjects research. Certification in research ethics or compliance, such as CITI Program training, is often required, and strong analytical and communication skills are essential for reviewing research protocols. Full-time IRB roles may also require familiarity with federal regulations like the Common Rule and institutional policies.

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 Full Time Irb jobs in Florida?

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

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

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

What cities in Florida are hiring for Full Time Irb jobs?

Cities in Florida with the most Full Time Irb job openings:

Full Time Irb jobs near you
Infographic showing various Full Time Irb job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

IRB Coordinator

BayCare Health System

Clearwater, FL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 days ago

BayCare Health System rating

7.4

Company rating: 7.4 out of 10

Based on 406 frontline employees who took The Breakroom Quiz

267th of 898 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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