Clinical Research Assistant

Responsibilities

• Participate in recruitment and pre-screening events to identify potential participants
• Conduct phone screenings and review medical records, study charts, and subject databases
• Assist with obtaining informed consent under the direction of the Clinical Research Coordinator (CRC)
• Complete visit procedures, collect, process, and ship specimens as required by protocol
• Record data accurately in real time on paper or electronic source documents
• Maintain site logs, inventory, and equipment supplies
• Ensure strict adherence to FDA regulations, ICH guidelines, and institutional SOPs
• Perform administrative tasks including filing, scanning, and updating internal recruitment trackers

Requirements

• Bilingual in Spanish (required)
• Minimum of 1 year of recent experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant, or Phlebotomist
• Proven proficiency in phlebotomy and blood draws
• Working knowledge of medical and research terminology
• Understanding of federal regulations and Good Clinical Practices (GCP)
• Proficiency in Microsoft Office Suite

Preferred Qualifications

• Previous experience working specifically within clinical drug trials

Benefits

• 100% employer-paid medical, dental, and vision insurance options
• Paid Time Off (PTO) and company-paid holidays
• 401(k) retirement plan with company match
• Health Savings Account (HSA) and Flexible Spending Account (FSA) options
• Company-paid Short-Term and Long-Term Disability

About the Company

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.