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Part Time Irb Jobs in Arizona (NOW HIRING)

DocTrials

Part-Time Optician (Research)

Chandler, AZ

$17 - $21.75/hr

DR Part-time positions available We're looking for an experienced and detail-oriented Optician to ... You'll help ensure compliance with all research and IRB standards. * Patient Care & Safety: Provide ...

DocTrials

Part-Time Optician (Research)

Chandler, AZ · On-site

$17 - $21.75/hr

DR Part-time positions available We're looking for an experienced and detail-oriented Optician to ... You'll help ensure compliance with all research and IRB standards. * Patient Care & Safety: Provide ...

DocTrials

Part-Time Optician (Research)

Chandler, AZ · On-site

$17 - $21.75/hr

DR Part-time positions available We're looking for an experienced and detail-oriented Optician to ... You'll help ensure compliance with all research and IRB standards. * Patient Care & Safety: Provide ...

University of Arizona

Project Coordinator

Tucson, AZ · On-site

$25.50 - $31.87/hr

Knowledge of research regulatory compliance (FDA/IHC-GCP) and IRB processes. * Knowledge of ... FLSA Non-Exempt Full Time/Part Time Part Time Number of Hours Worked per Week 30 Job FTE 0.75 Work ...

Mayo Clinic

Program Coordinator - Research

Phoenix, AZ · Hybrid

$33.39 - $50.13/hr

Experience supporting IRB submissions, regulatory compliance activities, and study start-up ... Benefits Eligible No Schedule Part Time Hours/Pay Period Supplemental/PRN; as needed based on ...

All JobsIrb JobsPart Time Irb JobsPart Time Irb Jobs in Arizona

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 Arizona?

The most popular types of Irb jobs in Arizona are:

What are popular job titles related to Part Time Irb jobs in Arizona?

For Part Time Irb jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Part Time Irb jobs in Arizona look for?

The top searched job categories for Part Time Irb jobs in Arizona are:

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

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

Part Time Irb jobs near you
Infographic showing various Part Time Irb job openings in Arizona as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution.

Part-Time Optician (Research)

DocTrials

Chandler, AZ

$17 - $21.75/hr

Part-time

Re-posted 27 days ago

Job description

TL;DR

Part-time positions available
We're looking for an experienced and detail-oriented Optician to support ongoing ophthalmic clinical trials at our research sites. This is a part-time position with a flexible schedule, ideal for someone who can adjust their availability based on patient visit schedules. You'll work closely with our study coordinators and investigators to perform key clinical trial assessments, ensuring data accuracy and patient safety while contributing to cutting-edge ophthalmic research.

This position is perfect for an Optician who enjoys patient care, values precision, and thrives in a dynamic environment. Experience in clinical research is a plus but not required-training and certification will be provided.


What You Will Own & Improve

  • Study Assessments: Perform protocol-required ophthalmic assessments, including refraction and visual acuity. You'll ensure all study procedures are conducted per protocol and GCP guidelines.
  • Certification & Compliance: Obtain and maintain all required study certifications (e.g., protocol-specific visual acuity, refraction, or imaging certifications). You'll help ensure compliance with all research and IRB standards.
  • Patient Care & Safety: Provide compassionate, professional care to research participants. Monitor for adverse events and communicate findings promptly to the study investigator.
  • Collaboration & Documentation: Work alongside the clinical research team to ensure efficient clinic flow, accurate source documentation, and timely data entry.
  • Flexible Scheduling: Availability to come in based on study visit schedules (patient appointments will vary by protocol).

What You Already Know

  • Licensed or experienced Optician (ABO certification preferred)
  • Strong understanding of optical dispensing, lens types, and frame adjustments
  • Familiar with refraction principles and visual acuity measurement (Snellen, ETDRS)
  • Excellent communication and organizational skills
  • Comfortable working with patients in a clinical setting
  • Prior experience in ophthalmology or research is a plus but not required


What You Will Learn

  • How to apply your optometric skills in a research environment
  • Protocol-specific certification and documentation requirements
  • Collaboration with sponsors, CROs, and regulatory teams
  • The ins and outs of ophthalmic clinical trial conduct, from screening through closeout

About the Team

You'll work alongside a small, dedicated clinical research team that includes physicians, coordinators, and ophthalmic technicians.
This role reports to the Director of Clinical Research or Site Manager.
Local travel to nearby clinic locations may occasionally be required.


Benefits at DocTrials

Competitive salary | Flexible schedule | Company adventures


Values at DocTrials

Align Your Daily Priorities | Roll Out the Red Carpet | Be Obsessed About Learning
Show Up Ready | What Can We Do? | Don't Panic
Don't Work in a Bubble | Recognize the Gray | Have a Positive Purpose


About Us

DocTrials' culture is guided by our values and behavior. Our success depends on how much we care for each other, our customers, and our community. DocTrials is an alliance of physician sites specializing in the conduct of clinical studies within their private practices. Sites in the alliance work under DocTrials' core standard operating procedures and quality control measures that provide a methodology ensuring the highest quality control and best practice utilization across sites. This provides assurance and confidence to sponsors that they will achieve quality data in the most efficient and timely manner. DocTrials was founded with the primary goal of connecting patients and physicians with clinical trials across the US; aiding in the process to discover new therapies, bring hope, and find new treatment for disease.

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