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Irb Research Associate Jobs (NOW HIRING)

BayCare Health System

IRB Coordinator

Clearwater, FL · On-site

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 ...

BayCare Health System

IRB Coordinator

Clearwater, FL · On-site

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 ...

Columbia University

Research Associate

Manhattan, NY

Research Associate Position Summary: This position entails coordinating flow of subject recruitment ... IRB-related tasks including amendments/exceptions; drafting and/or editing Standard Operating ...

Columbia University

Research Associate

Manhattan, NY

Research Associate Position Summary: This position entails coordinating flow of subject recruitment ... IRB-related tasks including amendments/exceptions; drafting and/or editing Standard Operating ...

Apex Informatics

Research Associate

Mountain View, CA · On-site

Research Associate ( W2 role) Loc : Onsite in San Francisco OR Mountain View - Independently run ... products. - Assisting IRB submissions, working with Google to facilitate Launch approvals ...

Brandeis University

Research Associate I

Waltham, MA · On-site

Brandeis University seeks to hire a Research Associate I who will contribute substantively to ... IRB communications; and tracking project budgets. This is a full-time grant funded position. The ...

Nourish

Research Associate

Seattle, WA · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

San Francisco, CA · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

Chicago, IL · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

Denver, CO · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

Boston, MA · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

New York, NY · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

New York, NY · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

New York, NY · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

Nourish

Research Associate

San Diego, CA · On-site +1

About the Role As our first Research Associate, you will play a foundational role in building the ... You'll design and execute IRB protocols for strategically important clinical studies, manage ...

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Irb Research Associate information

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How much do irb research associate jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for irb research associate in the United States is $32.54, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $37.02 per hour, depending on experience, location, and employer.

What is an IRB Research Associate?

IRB Research Associates are professionals who assist with the ethical review and oversight of research involving human subjects. They work closely with Institutional Review Boards (IRBs) to ensure that research proposals comply with federal regulations, institutional policies, and ethical standards. Their responsibilities often include reviewing research protocols, preparing documentation, communicating with researchers, and maintaining records of IRB deliberations and decisions. IRB Research Associates play a crucial role in protecting the rights and welfare of research participants.

What are some common challenges IRB Research Associates face when coordinating between researchers and the Institutional Review Board?

IRB Research Associates often navigate complex communication between researchers and the Institutional Review Board to ensure studies comply with ethical and regulatory requirements. A common challenge is balancing timely project progress with strict adherence to documentation and review processes, which can involve frequent follow-ups and clarifications. Associates must also interpret evolving regulations and help researchers adapt their study protocols accordingly, requiring strong attention to detail and collaborative skills. Successfully managing these dynamics fosters a culture of compliance while supporting innovative research.

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

To thrive as an IRB Research Associate, you need a thorough understanding of research ethics, human subjects protection regulations, and often a bachelor's or master's degree in a related field. Familiarity with IRB management systems, federal compliance databases, and regulatory documentation tools is typically required. Strong attention to detail, excellent written communication, and organizational skills help ensure effective protocol review and collaboration with researchers. These competencies are crucial for safeguarding participant welfare, maintaining regulatory compliance, and supporting ethical research practices.

What is the difference between Irb Research Associate vs Clinical Research Coordinator?

AspectIrb Research AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, sometimes certifications in research or ethicsBachelor's degree, often certifications in clinical research or Good Clinical Practice (GCP)
Work EnvironmentResearch labs, hospitals, academic institutionsHospitals, clinics, research sites
Employer & Industry UsageResearch institutions, biotech, pharmaHospitals, clinical trial sites, research organizations
Common Search & ComparisonOften compared for roles in research compliance and ethicsFocuses on patient coordination and trial management

The Irb Research Associate and Clinical Research Coordinator roles both involve clinical research but differ mainly in focus. The Irb Research Associate primarily handles ethics review and compliance, while the Clinical Research Coordinator manages patient recruitment and trial logistics. Both roles require similar educational backgrounds and certifications, often working within the healthcare and research industries.

How to become an IRB research associate?

To become an IRB research associate, candidates typically need a bachelor's degree in a health-related or research field, along with experience in research compliance or ethics. Familiarity with federal regulations such as the Common Rule and good organizational skills are also important. Some positions may require certification or training in research ethics or human subjects protection.

What are popular job titles related to Irb Research Associate jobs?

For Irb Research Associate jobs, the most frequently searched job titles are:

Infographic showing various Irb Research Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $67,685 per year, or $32.5 per hour.

Clinical Research Associate

Syracuse, NY • On-site

SUNY Upstate Medical University
Colleges, Universities, and Professional Schools • 1 - 5K employees
Learn more about SUNY Upstate Medical Universityexternal

$65K - $85K/yr

Full-time

Posted 14 days ago

SUNY Upstate Medical University rating

8.1

Company rating: 8.1 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

Job description

Clinical Research Associate

 

Job Summary:

SUNY Upstate Pediatrics Team is in search of a Clinical Research Associate II who will coordinate Clinical Research studies in the Division of Pediatric Infectious Diseases.

The CRA II will facilitate and coordinate the daily clinical trial activities and will play a critical role in the conduct of the studies. The CRA will work with the PI, the Pediatric infectious Diseases Division, Staff, study,sponsors and tech institutional IRB, research accounting, CTO, etc. to provide guidance, coordination, compliance, financial and other related aspects of clinical trials activity. The research interests in the Pediatric ID Division are vaccinology and viral epidemiology and pathogenesis of Pediatric Respiratory Tract Infections.

Key Responsibilities:

  • Patient interview and education to determine eligibility for clinical trial
  • Manage data collection and recording for clinical trials, data base maintenance for clinical trials,and oversight of research supplies.
  • provide patient education, eligibility assessment and enrollment as
  • responsible for clinical trials billing to ensure timely submission and
  • Coordination of budget negotiations, coordinates study auditor visits, filing reports to studysponsors and IRB, maintain budget and process
  • Completion and maintenance of study related documentation and monitoring requirements
  • Coordinator for at least one research study, including IRB
  • Will report adverse events to the study sponsors the IRB as required in a timely manner.

Minimum Qualifications:

Bachelor's Degree in Nursing with 3 years of Clinical Research Experience. NYS RN License at time of appointment.

Preferred Qualifications:

A Licensed Advanced Practice Nursing professional preferred.

Work Days:

Monday - Friday, Days

Message to Applicants:

Salary Range: $65,000 - $85,000, DOE

Why Join Research Foundation.pdf

Recruitment Office: Human Resources

Please consider applying to our current opportunity at https://careers.upstate.edu/ Job# 90145

 

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status or disability.

Company Description

Upstate Medical University, Syracuse, NY.
We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status or disability.

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