What are the responsibilities and job description for the Clinical Research Coordinator - Bilingual position at SQRL?
HIGHLIGHTS
- Full-time, Monday–Friday schedule (8 AM–5 PM), with occasional paid overtime on weekends or evenings
- Competitive hourly pay comprehensive benefits, PTO, and 401k match
- Work with cutting-edge clinical trials in multiple therapeutic areas
- Opportunity to grow in a rapidly expanding research network
- Bilingual Spanish/English required
COMPANY
Our client is a fast-growing clinical research site network with 31 sites across 9 states, known for offering career development and growth opportunities in an entrepreneurial, patient-centered environment. They are driven by a mission to change lives through innovative research while fostering a diverse and inclusive workplace. With continued expansion planned for 2025 and beyond, this is a great place to build a meaningful, long-term career.
POSITION
We’re seeking a Bilingual Clinical Research Coordinator for our client’s Leesburg, FL location. In this role, you’ll support a wide variety of clinical trials from start to finish, ensuring the highest quality care for participants and compliance with regulatory standards. You’ll be a key player in both the operational and patient-facing aspects of research, making a direct impact on trial success.
RESPONSIBILITIES
- Guide patients through the informed consent process with clarity and empathy
- Execute study protocols with precision, including EKGs, vitals, and phlebotomy
- Collect, process, and ship human specimens accurately
- Maintain clean and complete electronic source documentation (e-source)
- Communicate with sponsors and CROs to ensure seamless study operations
- Participate in site monitoring and initiation visits
- Ensure regulatory and GCP compliance across all trial activities
QUALIFICATIONS
- Bilingual in Spanish and English
- Phlebotomy experience required; EKG or other lab experience a plus
- Previous experience as a Clinical Research Coordinator (1 years preferred)
- Familiarity with FDA, ICH-GCP guidelines, and electronic data systems
- Strong communication, critical thinking, and attention to detail
- Bachelor’s degree preferred, but not required
