ZipRecruiter

Log In

2

Irb Manager Part Time Jobs (NOW HIRING)

Aptive

Management Analyst

Job Summary Aptive Resources is seeking a management consultant with demonstrated research and ... IRB, NIH, VA). This is 100% remote position, with an option as either full-time or part-time. ...

DocTrials

Part-Time Optician (Research)

Chandler, AZ

$17 - $21.75/hr

You'll help ensure compliance with all research and IRB standards. * Patient Care & Safety: Provide ... This role reports to the Director of Clinical Research or Site Manager. Local travel to nearby ...

DocTrials

Part-Time Optician (Research)

Chandler, AZ · On-site

$17 - $21.75/hr

Youll help ensure compliance with all research and IRB standards. * Patient Care & Safety: Provide ... This role reports to the Director of Clinical Research or Site Manager. Local travel to nearby ...

DocTrials

Part-Time Optician (Research)

Chandler, AZ · On-site

$17 - $21.75/hr

You'll help ensure compliance with all research and IRB standards. * Patient Care & Safety: Provide ... This role reports to the Director of Clinical Research or Site Manager. Local travel to nearby ...

Unf

Part-Time Research Associate

Jacksonville, FL · On-site +1

$35/hr

MedNexus Research Innovation Fund Support * Assist with the management, growth, and tracking of the ... Familiarity with program evaluation methods and IRB processes. * Previous involvement in innovation ...

The University of Miami

Research Associate 1

Miami, FL · On-site +1

... part time Research Associate 1. The Research Associate 1 supports research activities for the ... The provided research role involves managing the end-to-end qualitative research process, from ...

University of Miami

Research Associate 1

Miami, FL

... part time Research Associate 1. The Research Associate 1 supports research activities for the ... The provided research role involves managing the end-to-end qualitative research process, from ...

next page

Showing results 1-20

All JobsIrb JobsIrb Manager Part Time Jobs

Irb Manager Part Time information

See salary details

$58.5K

$78.6K

$99.5K

How much do irb manager part time jobs pay per year?

As of Jul 11, 2026, the average yearly pay for irb manager part time in the United States is $78,591.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $81,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an IRB Manager (Part Time), and why are they important?

To thrive as an IRB Manager (Part Time), you need in-depth knowledge of federal regulations for human subjects research, experience in research compliance, and typically a bachelor’s or master’s degree in a related field. Familiarity with electronic IRB management systems and certifications such as CIP (Certified IRB Professional) are highly valuable. Exceptional organizational skills, attention to detail, and strong interpersonal communication are crucial soft skills for success in this role. These skills ensure ethical oversight, regulatory compliance, and effective coordination between researchers and the Institutional Review Board.

What does an IRB Manager do in a part-time role?

An IRB (Institutional Review Board) Manager in a part-time role oversees the review and approval process for research involving human subjects to ensure compliance with ethical standards and federal regulations. Their responsibilities typically include coordinating IRB meetings, reviewing research protocols, ensuring proper documentation, and providing guidance to researchers. Even part-time IRB Managers play a crucial role in safeguarding participant rights and maintaining research integrity, often balancing administrative duties with regulatory compliance tasks.

What are some common challenges faced by part-time IRB Managers when balancing compliance oversight with limited hours?

Part-time IRB Managers often encounter the challenge of maintaining thorough oversight of research protocols and ensuring timely review processes within a reduced work schedule. Effective time management and prioritization are essential, especially during periods of high submission volume or when new regulations are introduced. Frequent communication and clear delegation with IRB staff and committee members help maintain workflow continuity. Staying organized and leveraging digital management tools can also support compliance and efficiency despite limited hours.
More about Irb Manager Part Time jobs
What cities are hiring for Irb Manager Part Time jobs? Cities with the most Irb Manager Part Time job openings:
What job categories do people searching Irb Manager Part Time jobs look for? The top searched job categories for Irb Manager Part Time jobs are:
Irb Manager Part Time jobs near you
Infographic showing various Irb Manager Part Time job openings in the United States as of July 2026, with employment types broken down into 48% Full Time, 7% Part Time, 1% Contract, 41% Nights, and 3% Summer. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $78,591 per year, or $37.8 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

Re-posted 29 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: