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Clinical Study Assistant Jobs in Arizona (NOW HIRING)

MMS

Senior Medical Writer (Remote)

Phoenix, AZ · On-site

... that will assist our clients in developing and marketing life-changing therapies to positively ... Substantial clinical study protocol experience, as lead author, required * Experience leading and ...

Headlands Research

Clinical Research Assistant

Scottsdale, AZ

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform intramuscular injections for vaccine studies, when necessary * Assist research coordinators in conducting clinical trial visits in compliance with study protocols * Collect and record vital ...

Stereotaxis

Territory Assistant

Phoenix, AZ · On-site

$18.50 - $24.25/hr

Learn key clinical, workflow, and equipment involved in EP procedures, through case observations, guided instruction and simulator sessions, and independent study. Assist with system maintenance and ...

Headlands Research

Clinical Research Assistant

Scottsdale, AZ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform intramuscular injections for vaccine studies, when necessary * Assist research coordinators in conducting clinical trial visits in compliance with study protocols * Collect and record vital ...

DM Clinical

Clinical Research Coordinator I (3932)

Phoenix, AZ · On-site

$23 - $30.50/hr

The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure ... Registered Medical Assistant certification or equivalent is preferred Knowledge and Skills: * Be an ...

Actalent

Clinical Research Coordinator

Phoenix, AZ · On-site

$58K - $68K/yr

Coordinate day-to-day clinical trial operations in accordance with study protocols and regulatory requirements. * Assist with patient recruitment by identifying, contacting, and engaging potential ...

ALLIANCE CLINICAL LLC

Clinical Research Coordinator I

Phoenix, AZ · On-site

$24 - $32/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Communicate clearly and professionally with study participants regarding study objectives and ... At least 1 year of experience with phlebotomy and EKG procedures, or a Medical Assistant ...

Care Access

Clinical Research Assistant

Mesa, AZ

$19 - $33/hr

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical ... Maintain effective relationships with study participants and other care Access Research personnel ...

Az Asthma & Allergy Institute

Medical Assistant

Mesa, AZ · On-site

$15.50 - $20/hr

REQUIRED - YOU MUST HAVE A MEDICAL ASSISTANT DIPLOMA OR CERTIFICATION. Reports To: MA Coordinator ... Other Requirements Be able to complete AAAI administered clinical study guidesand pass exams on ...

Care Access

Clinical Research Assistant

Mesa, AZ · On-site

$19 - $33/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

How This Role Makes a Difference The Clinical Research Assistant is an entry level clinical ... Request study participant payments * Schedule visits with participants, contact with reminders

Az Asthma & Allergy Institute

Medical Assistant

Peoria, AZ · On-site

$17.50 - $22.50/hr

Confirm medications and key elements of medical history, document any changes. * Assist the ... Other Requirements Be able to complete AAAI administered clinical study guidesand pass exams on ...

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All JobsClinical Study JobsClinical Study Assistant JobsClinical Study Assistant Jobs in Arizona

Clinical Study Assistant information

See Arizona salary details

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How much do clinical study assistant jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical study assistant in Arizona is $18.85, according to ZipRecruiter salary data. Most workers in this role earn between $15.48 and $21.73 per hour, depending on experience, location, and employer.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

What is the difference between Clinical Study Assistant vs Clinical Research Coordinator?

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What are the most commonly searched types of Clinical Study jobs in Arizona?

The most popular types of Clinical Study jobs in Arizona are:

What cities in Arizona are hiring for Clinical Study Assistant jobs?

Cities in Arizona with the most Clinical Study Assistant job openings:

Clinical Study Assistant jobs near you
Infographic showing various Clinical Study Assistant job openings in Arizona as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 15% Part Time, 2% Temporary, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $39,213 per year, or $18.9 per hour.

Bilingual Clinical Research Assistant (Spanish/English)

DocTrials

Phoenix, AZ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 25 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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