Research Assistant (Clinical) Scottsdale, Arizona

Headlands Research, Inc.

Scottsdale, AZFull-timePosted Apr 7, 2026

Behavioral Health Market Context

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Benefits

Health InsuranceDental CoveragePaid Time Off

Job Description

linical Research Assistant (non-lab)
We’re seeking a Clinical Research Assistant (RA) for our clinical research site located in Scottsdale. As an RA, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.

The Role:

As a Clinical Research Assistant, you’ll work side‑by‑side with experienced Clinical Research Coordinators, Investigators, and cross‑functional teams to support all aspects of clinical trial execution—from subject screening to data entry. Your work will directly contribute to the success of new treatments in development.

Type: Regular Full‑time Employee
Schedule: Mondays through Fridays, 8:00 am – 5:00 pm
Location: Onsite in Scottsdale, AZ (no remote or hybrid work)
Reports to: Site Director
Benefits: Our benefits package for full‑time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

What We Offer

Competitive pay + annual performance incentives

Medical, dental, and vision insurance

401(k) plan with company match

Paid time off (PTO) and company holidays

Opportunities for professional development and career growth

A mission‑driven culture focused on advancing medicine and improving patient outcomes

Responsibilities :

Assist research coordinators in conducting clinical trial visits in compliance with study protocols

Collect and record vital signs, make study‑related phone calls, and document data in electronic systems

Support subject screening, enrollment , and follow‑up processes

Review and verify study documentation for accuracy and completeness

Maintain close communication with coordinators, investigators, and study participants

Requirements :

Familiarity with medical terminology required

Prior experience providing direct hands‑on patient care required

Clinical research experience preferred

Strong attention to detail, time management, and ability to work in a fast‑paced, regulated environment

Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors

Passion for improving patient outcomes through research

As set forth in Headlands Research’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.

#J-18808-Ljbffr Headlands Research, Inc.

Qualifications

  • Familiarity with medical terminology required
  • Prior experience providing direct hands‑on patient care required
  • Strong attention to detail, time management, and ability to work in a fast‑paced, regulated environment
  • Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors
  • Passion for improving patient outcomes through research

Benefits

  • Schedule: Mondays through Fridays, 8:00 am – 5:00 pm
  • Benefits: Our benefits package for full‑time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • Opportunities for professional development and career growth

Responsibilities

  • As a Clinical Research Assistant, you’ll work side‑by‑side with experienced Clinical Research Coordinators, Investigators, and cross‑functional teams to support all aspects of clinical trial execution—from subject screening to data entry
  • Your work will directly contribute to the success of new treatments in development
  • Type: Regular Full‑time Employee
  • Assist research coordinators in conducting clinical trial visits in compliance with study protocols
  • Collect and record vital signs, make study‑related phone calls, and document data in electronic systems
  • Support subject screening, enrollment , and follow‑up processes
  • Review and verify study documentation for accuracy and completeness
  • Maintain close communication with coordinators, investigators, and study participants


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