Research Assistant (Clinical) Scottsdale, Arizona
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.
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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