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Part Time Clinical Research Rater Jobs in Gilbert, AZ

DocTrials

Part-Time Optician (Research)

Chandler, AZ · On-site

$17 - $21.75/hr

DR Part-time positions available Were looking for an experienced and detail-oriented Optician to ... Experience in clinical research is a plus but not requiredtraining and certification will be ...

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 ... Experience in clinical research is a plus but not required--training and certification will be ...

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 ... Experience in clinical research is a plus but not required-training and certification will be ...

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 ... Experience in clinical research is a plus but not required-training and certification will be ...

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Part Time Clinical Research Rater information

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How much do part time clinical research rater jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for part time clinical research rater in Gilbert, AZ is $22.64, according to ZipRecruiter salary data. Most workers in this role earn between $17.26 and $25.87 per hour, depending on experience, location, and employer.

What is a part time clinical research rater?

A Part Time Clinical Research Rater is a professional who assists in clinical research studies by administering assessments, collecting data, and evaluating participants under the supervision of a research team. Their primary responsibilities include conducting interviews, scoring standardized tests, and documenting findings accurately. Working part-time, they often have flexible hours and may work on multiple studies at once. This role is important for ensuring data quality and reliability in clinical trials, particularly in areas like psychology, psychiatry, and neurology.

What are the key skills and qualifications needed to thrive as a part time clinical research rater?

To thrive as a Part Time Clinical Research Rater, you need a background in psychology, nursing, or a related field and experience with clinical assessments or research protocols. Familiarity with electronic data capture systems, standardized rating scales (e.g., HAM-D, MADRS), and basic statistical software is typically required. Attention to detail, strong organizational skills, and effective communication help ensure accuracy and integrity in data collection. These skills are crucial for delivering reliable research results and maintaining high-quality study standards.

What is the difference between Part Time Clinical Research Rater vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical Research RaterPart Time Clinical Research Coordinator
CredentialsTypically requires a high school diploma or equivalent; some roles prefer healthcare or research experienceRequires a bachelor's degree in health sciences or related field; certification may be preferred
Work EnvironmentRemote or flexible settings, focusing on assessments and data collectionClinical sites or research facilities, overseeing study procedures and participant management
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for data collectionEmployed by hospitals, research institutions, and pharmaceutical companies to coordinate studies

While both roles support clinical research, Part Time Clinical Research Raters primarily focus on evaluating participants' responses and data collection remotely, whereas Part Time Clinical Research Coordinators manage study logistics and participant interactions on-site. The roles differ in responsibilities, required credentials, and work environment, but both contribute to the successful conduct of clinical trials.

How does a part time clinical research rater typically collaborate with other members of a research team?

As a Part Time Clinical Research Rater, you will work closely with clinical coordinators, principal investigators, and other raters to ensure consistent and accurate data collection. Collaboration often involves regular meetings to discuss study protocols, review rating scales, and resolve discrepancies in assessments. Effective communication is key, as you may need to clarify procedures, share observations, and update the team on participant progress. This teamwork ensures the integrity of study data and contributes to the overall success of clinical trials.
What are the most commonly searched types of Clinical Research Rater jobs in Gilbert, AZ? The most popular types of Clinical Research Rater jobs in Gilbert, AZ are:
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Part Time Clinical Research Rater jobs near you
Infographic showing various Part Time Clinical Research Rater job openings in Gilbert, AZ as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $47,090 per year, or $22.6 per hour.

Bilingual Clinical Research Assistant (Spanish/English)

DocTrials

Phoenix, AZ • On-site

Part-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 18 days ago

Job description

TL;DR

Northwest Valley & Phoenix locations

Full & part time available


As a Clinical Research Assistant, you love to-do lists, organization, and are a master of administrative tasks. You have pronounced attention to detail and are obsessed with learning. As a lifelong seeker of knowledge you read everything! Patient care and excellent bedside manner is a top priority for you. When faced with a challenge, you take a breath, grab your resources, and make a plan! Preparation, agendas, and crushing tasks are your jam. You are an eager self-starter who wants to develop a strong foundation to grow as a Clinical Research Coordinator. You may or may not have some previous clinical research experience and/or ophthalmology experience. Fluency in English and Spanish required. Bachelor's degree preferred.

What you will own & improve

  • Patient acquisition: You will be responsible for reviewing patient charts for enrolling trials, creating telephone screening sheets, and conducting recruitment calls. You may also schedule and support with lunch n' learn and other community outreach activities.
  • Patient chart maintenance: You will be responsible for scanning, filing, and completing tasks within Clinical Trial Management Software (CTMS).
  • Process important study information. Relay information from study bulletins, newsletters, and memos to the team by utilizing a project management platform, Basecamp.
  • Site organization and upkeep. Manage study supplies, inventory, prepping, and ordering.
  • Vitals and laboratory. You will be responsible for collecting patient vitals and performing laboratory assessments.
  • Clinic flow. Like a clinic ninja, you will manage the task of quickly and efficiently moving patients through protocol assessments.


What you already know

  • How to engage with patients, deliver excellent customer service, and roll out the red carpet!
  • You know your way around a computer, printer, scanner - the basics. You also consider yourself tech savvy and pick up on new platforms quickly.
  • How to make the most out of any space; no matter how small. You consider organizing a hobby and probably have a personal label maker.
  • Previous experience in the medical field (ophthalmology or other) is a major plus!

What you will learn

  • You will establish a strong foundation of skills to grow as a Clinical Research Coordinator in order to conduct complex interventional & therapeutic protocols in compliance with FDA regulations and ICH-GCP guidelines.
  • How to conduct patient acquisition to meet and exceed enrollment goals.
  • How to cultivate a positive working relationship with all of our customers (Sponsor/CRO & Physician Specialists).

About the Team

This role reports to our Director of Clinical Research or Site Manager.

Local Travel required.

Benefits at DocTrials

Competitive salary

Health insurance

Dental & vision

Paid time off

Retirement plan

Flexible scheduling

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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