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Part Time Irb Jobs in Florida (NOW HIRING)

... part-time Research Associate to support research, program evaluation, and innovation-focused ... Familiarity with program evaluation methods and IRB processes. * Previous involvement in innovation ...

Part Time Irb information

What is a part-time IRB?

Part-time IRB (Institutional Review Board) professionals are individuals who work on a less-than-full-time basis to oversee the ethical review of research involving human subjects. Their responsibilities typically include reviewing research protocols, ensuring compliance with ethical standards, and protecting the rights and welfare of research participants. Part-time IRB members or staff may work for universities, hospitals, or other research institutions and often balance these duties with other professional roles. This flexible arrangement allows organizations to utilize their expertise without requiring a full-time commitment.

What are the typical responsibilities of a part-time IRB?

In a part-time IRB position, your primary responsibilities often include reviewing research proposals to ensure ethical standards are met, participating in regular board meetings, and providing feedback to researchers on compliance with regulations. You may also assist with training new members and staying updated on policy changes. Collaboration with other IRB members and administrative staff is common, and balancing review deadlines with a part-time schedule can be a key challenge. This role offers valuable exposure to research ethics and can be a stepping stone to more advanced regulatory or research administration positions.

What skills and qualifications are needed to thrive as a part-time IRB?

To thrive as a part-time IRB member, you need a solid understanding of research ethics, regulatory compliance, and human subjects protection, often supported by relevant academic or professional experience. Familiarity with IRB management software, federal regulations (such as the Common Rule), and certifications like CITI Program training is typically required. Strong analytical skills, attention to detail, and the ability to communicate complex ethical considerations clearly are essential soft skills. These competencies ensure that research proposals are reviewed thoroughly, ethically, and in accordance with legal standards to protect research participants.

What is the difference between Part Time Irb vs Part Time Research Coordinator?

AspectPart Time IrbPart Time Research Coordinator
Required CredentialsTypically requires IRB certification or training, understanding of ethical guidelinesRequires research experience, often with familiarity in IRB processes, but may not need certification
Work EnvironmentPrimarily administrative, reviewing research protocols for complianceMore hands-on with study management, participant interaction, and data collection
Employer & Industry UsageUsed by research institutions, hospitals, and universities for ethical reviewEmployed by research sites, hospitals, and academic institutions to coordinate studies

While both roles are involved in research, Part Time Irb focuses on ethical review and compliance, whereas Part Time Research Coordinator handles study operations and participant management. Understanding these differences helps job seekers target the right position based on their skills and interests.

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

The most popular types of Irb jobs in Florida are:

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

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

Infographic showing various Part Time Irb job openings in Florida as of August 2026, with employment types broken down into 100% Part Time. Highlights an 67% In-person, and 33% Remote job distribution.

OPS Clinical Research Nurse

University of Florida

Gainesville, FL • On-site

$30 - $40/hr

Part-time

Posted 4 days ago


University Of Florida rating

7.2

Company rating: 7.2 out of 10

Based on 108 frontline employees who took The Breakroom Quiz

386th of 620 rated colleges and universities


Job description

OPS Clinical Research Nurse
Job no: 540186
Work type: Temp Part-Time
Location: Main Campus (Gainesville, FL)
Categories: Nursing, Health Care Administration/Support
Department:29680300 - MD-CTSI-CLINICAL RESEARCH CNTR
Classification Title:
OPS Clinical Research Nurse
Classification Minimum Requirements:
Graduate of a nationally accredited nursing program and four years of professional nursing experience. Licensed as a registered nurse in accordance with Chapter 464, Florida Statutes.
Job Description:
The Clinical and Translational Science Institute (CTSI) is seeking an OPS Clinical Research Nurse to conduct and assist in the organization of our clinical research program. The incumbent will conduct examinations and administer treatments and/or medications in accordance with research protocols. Research activities may occur in the Clinical Research Center (CRC) located in the Clinical and Translational Science Building (CTRB), Shands Hospital or in various UF clinics.
About this role:
Provide nursing care and education in support of clinical research trials and projects in clinical settings:
  • Provide clinical care to participants enrolled in clinical trials.
  • Perform assessments, such as vital signs, in accordance with research protocols
  • Administer treatments and/or investigational medications in accordance with research protocols.
  • Initiate ordering of necessary tests, equipment and medications per protocol.
  • Perform specialized tasks such as pharmacokinetic sampling, administration of conscious sedation; assisting with invasive procedures such as liver biopsies and bronchoscopies.
  • Collect body fluid specimens, including timed specimens for pharmacokinetic assessments.
  • Processes specimens for storage and shipping as required by protocol

Provide Administrative support to assigned research trials and projects:
  • Provide administrative support to NIH's WebCAMP scheduling and data tracking system.
  • Maintain detailed records of clinical research trials and projects, including data collection, while maintaining HIPAA compliance standards regarding patient confidentiality.
  • Alert Principal Investigator(s) to any Adverse Events/Serious Adverse Events for timely reporting to the IRB when appropriate.
  • Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals.

Provide logistical support to the Clinical Research Center in support of research trials and projects:
  • Assist with stocking and supplies of unit, ensuring supplies are in date and stocked, ensuring unit readiness.
  • Assist with maintaining equipment including daily checks.
  • Assist with scheduling of participants on WebCAMP system.
  • Maintain and update billing for services provided on WebCAMP system.
  • Meet with study teams as needed for the coordination of services.

Lab Coverage:
  • On a rotating schedule, provide coverage in CRC Lab and assists as needed.

Training and Education:
  • Maintain compliance with Good Clinical Practice guidelines and Food and Drug Administration's regulations on all research activities.
  • Participate in in-services and research-specific training to update on new protocols entering clinic.
  • Continually participate in protocol reading and updates to familiarize with current protocols.
  • Participate in unit-wide trainings to keep up-to-date research-specific skills.

Expected Salary:
$30.00-$40.00/hr; commensurate on education and experience.
Required Qualifications:
Graduate of a nationally accredited nursing program and four years of professional nursing experience. Licensed as a registered nurse in accordance with Chapter 464, Florida Statutes.
Preferred:
  • Nursing experience in a clinical research setting
  • ACLS certification
  • Knowledgeable regarding IRB procedures, forms and approval process
  • Knowledge of nursing principles, practices and techniques
  • Knowledge of basic principles and good clinical practice of clinical research
  • Experience coordinating clinical research studies
  • Skill in the use of nursing equipment and instruments
  • Ability to collect, collate, analyze and evaluate data from clinical research studies
  • Ability to plan, organize and coordinate work assignments
  • Ability to work effectively and independently
  • Ability to communicate effectively, both verbally and in writing
  • Expertise in phlebotomy

Special Instructions to Applicants:
In order to be considered, you must upload your cover letter and resume.
This requisition has been extended. Previous applicants are still under consideration and need not apply.
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required:Yes
Advertised: 18 Aug 2026 Eastern Daylight Time
Applications close: 25 Aug 2026 Eastern Daylight Time
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About University of Florida

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The University of Florida is one of the top ranked public universities in the United States (ranked top 5 amongst public universities in 2023 US news and world report). It is one of only a few comprehensive universities, having medical, veterinary, dental, nursing, public health, and engineering disciplines all co-localized on the same, contiguous campus to facilitate interdisciplinary collaboration. Gainesville is located in the northern region of Florida, within 1-1.5 hours of each coast, and just 1.5-2 hours to Orlando and Tampa. It is a small to medium-sized city with a low cost of living, excellent public and private schools, and southern hospitality. While Gainesville is widely recognized as the home of the Gators, it is quickly becoming known as a center for innovation and a place with a lifestyle that's comfortable for families, yet attractive for young professionals.

Industry

Colleges, universities, and professional schools

Company size

5,001 - 10,000 Employees

Headquarters location

Gainesville, FL, US

Year founded

1853