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Temp Irb Analyst Jobs (NOW HIRING)

Uw

Research Coordinator - Fixed Duration

Seattle, WA

$90K/yr

Complete IRB reports and annual reviews and regular reporting to funding agencies; and perform ... Manage and analyze data and prepare results for publication. - 15% * Other administrative ...

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University of Miami

Research Assistant 1, Per Diem

Miami, FL

$18.50 - $25.25/hr

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... Ability to analyze, organize and prioritize work under pressure while meeting deadlines. * Ability ...

UNC-Chapel Hill

Research Specialist

Chapel Hill, NC

$30/hr

... Temporary Staff (SHRA) Position Title Research Specialist Position Number 20076739 Vacancy ID ... specifying analyses), helping manage various aspects of quantitative projects (e.g., IRB ...

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Temp Irb Analyst information

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$73.3K

$130K

How much do temp irb analyst jobs pay per year?

As of Jun 11, 2026, the average yearly pay for temp irb analyst in the United States is $73,261.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $87,000.00 per year, depending on experience, location, and employer.

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

AspectTemp Irb AnalystClinical Research Coordinator
CredentialsBachelor's degree, IRB trainingBachelor's degree, clinical research training
Work EnvironmentOffice, regulatory agenciesClinical sites, hospitals
Industry UsageResearch institutions, pharmaHospitals, research sites
Primary FocusIRB review, complianceParticipant management, study coordination

The Temp Irb Analyst primarily focuses on IRB submissions and regulatory compliance, working closely with research protocols. In contrast, a Clinical Research Coordinator manages participant recruitment, scheduling, and day-to-day study activities. While both roles support clinical research, the Irb Analyst emphasizes regulatory review, whereas the Coordinator handles operational tasks at research sites.

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What cities are hiring for Temp Irb Analyst jobs? Cities with the most Temp Irb Analyst job openings:
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What job categories do people searching Temp Irb Analyst jobs look for? The top searched job categories for Temp Irb Analyst jobs are:
Temp Irb Analyst jobs near you
Infographic showing various Temp Irb Analyst job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 92% Full Time, 5% Part Time, and 2% Temporary. Highlights an 81% Physical, 8% Hybrid, and 11% Remote job distribution, with an average salary of $73,261 per year, or $35.2 per hour.
Clinical Research Coordinator I (Temporary/Part-Time)

Clinical Research Coordinator I (Temporary/Part-Time)

INBIOS INTERNATIONAL INC

Seattle, WA • On-site

$26.44 - $31.25/hr

Part-time, Temporary

Medical, Dental, Vision, Life, Retirement

Posted 28 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


Apply Today

Be part of a team that’s advancing science and improving lives.

Requirements: