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Entry Level Irb Analyst information

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$54

How much do entry level irb analyst jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for entry level irb analyst in the United States is $27.77, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $30.05 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Irb Analyst vs Clinical Research Coordinator?

AspectEntry Level Irb AnalystClinical Research Coordinator
Required CredentialsBachelor's degree, familiarity with IRB processesBachelor's degree, experience in clinical trial management
Work EnvironmentOffice-based, regulatory compliance focusClinical sites, patient interaction, trial coordination
Employer & Industry UsageHospitals, research institutions, biotech firmsHospitals, research centers, pharmaceutical companies

While both roles involve clinical research, an Entry Level Irb Analyst primarily focuses on regulatory review and IRB submissions, working in an office setting. In contrast, a Clinical Research Coordinator manages trial logistics and patient interactions at clinical sites. Both roles require a bachelor's degree, but the Coordinator role often demands more direct patient contact and trial management experience.

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What cities are hiring for Entry Level Irb Analyst jobs? Cities with the most Entry Level Irb Analyst job openings:
What are the most commonly searched types of Irb Analyst jobs? The most popular types of Irb Analyst jobs are:
What job categories do people searching Entry Level Irb Analyst jobs look for? The top searched job categories for Entry Level Irb Analyst jobs are:
Entry Level Irb Analyst jobs near you
Infographic showing various Entry Level Irb Analyst job openings in the United States as of June 2026, with employment types broken down into 40% Full Time, and 60% Part Time. Highlights an 100% In-person job distribution, with an average salary of $57,761 per year, or $27.8 per hour.
Clinical Research Coordinator I (Temporary/Part-Time)

Clinical Research Coordinator I (Temporary/Part-Time)

INBIOS INTERNATIONAL INC

Seattle, WA • Hybrid

$26.44 - $31.25/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 25 days ago

Job description

Description

Are you a detail-oriented problem-solver with a passion for purpose-driven work? Join InBios, a mission-focused biotech company developing diagnostic tools that combat infectious diseases worldwide.


About Us

InBios International Inc. has been in business since 1996 designing and manufacturing diagnostic assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded research, with a strong emphasis on innovation, quality, and compliance. Based in Seattle, we offer a collaborative culture, competitive compensation, and meaningful work that makes a global impact.


Location: Seattle, WA


Type: Part-Time (30 hours per week), Temporary (6-months) | Hybrid
This is a project-based position funded by a federal contract. If selected for the position, you will be hired as a temporary, part-time employee and the term of employment is dependent upon ongoing funding.


Position Wage Range:  $26.44 - $31.25/per hour


What You'll Do

We're looking for a temporary, part-time Clinical Research Coordinator to support clinical studies and international product registration. The successful candidate must have a BS in a scientific discipline, have familiarity with Good Clinical Practice (GCP) and have excellent attention to details as well as good communication skills but written and verbal. 


Key ResponsibilitiesClinical Site Monitoring
  • Under the direction of the Project Manager assist in the maintenance of regulatory binders and Institutional Review Board (IRB) submissions.
  • Monitor clinical study to ensure that all participant records entered into the electronic data capture system are accurate and follow the clinical protocol and source documents.
  • Participate in Site Initiation training (SIV), monitor study compliance, and assist with study closeout.
  • Ensure that participants enrolled in the study meet the inclusion/exclusion criteria.
  • Monitor and report protocol deviations and adverse events in a timely manner.
  • Participate in study site close-out.
Product Registrations (International)
  • Identify regulatory requirements for product registrations worldwide.
  • Review analytical and clinical data against country regulatory requirements and identify gaps that need to be filled to obtain product registration.
  • Assist in the preparation of technical files in compliance with IVDR.
What We're Looking ForRequired
  • Bachelor's degree in a scientific discipline.
  • Strong attention to detail, excellent written and verbal communication, and proficiency with technology (e.g., MS Office, Electronic Database Systems).
  • Knowledge of ICH GCP guidelines. GCP certification. 
  • Entry-level knowledge of IVDR requirements for medical devices. 
Preferred
  • 1- to 3-year experience in project management.
  • Certified Clinical      Research Associate credential.
Perks & Benefits
  • Medical, dental, vision, life & disability insurance
  • 401(k) + Roth IRA + FSA
  • Prorated paid holidays and sick time as applicable to term of employment and work schedule in accordance with policies stated in the Company's employee handbook.
  • Supportive, mission-driven culture


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