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Overview
Mid-Level

Clinical Research Assistant (Bilingual in Spanish)

Confirmed live in the last 24 hours

Care Access

Care Access

Compensation

$19.00 - $33.00/hr

Dalton, Georgia, United States
On-site
Posted April 6, 2026

Job Description

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com.

How This Role Makes a Difference

The Clinical Research Assistant is an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization. 

How You'll Make An Impact

  • Ability to understand and follow institutional SOPs   
  • Participate in recruitment and pre-screening events (may be at another location) 
  • Assist with preparation of outreach materials  
  • Identify potential participants by reviewing medical records, study charts and subject database   
  • Assist with recruitment of new participants by conducting phone screenings  
  • Request medical records of potential and current research participants   
  • Schedule visits with participants, contact with reminders   
  • Obtain informed consent per Care Access Research SOP, under the direction of the CRC 
  • Complete visit procedures as required by protocol, under the direction of the CRC 
  • Collect
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