Job Description

HIGHLIGHTS

• Full-time opportunity with consistent weekday schedule (Monday–Friday, 7:00 AM – 3:30 PM)
• Comprehensive benefits including health insurance, PTO, and 401k match
• Join a thriving research network with long-term growth potential
• Hands-on work supporting impactful clinical trials across multiple phases
• Collaborative, inclusive, and mission-driven culture

COMPANY

Our client is one of the fastest-growing site networks in the country, with 31 locations across 9 states—and they’re not slowing down. With a strong focus on career development, diversity, and advancing medical research, this organization offers a unique opportunity to grow your career while contributing to meaningful, life-changing work.

POSITION

We’re seeking a Clinical Research Coordinator to join our client’s Boca Raton, FL team. In this role, you’ll assist with the execution of clinical trials across various phases and therapeutic areas. You’ll work closely with patients, investigators, and sponsors to ensure protocol compliance and a high-quality research experience.

RESPONSIBILITIES

• Coordinate and conduct study visits in accordance with protocol, GCP, and regulatory guidelines
• Obtain informed consent from study participants and ensure documentation is complete
• Perform lab draws, EKGs, specimen processing, and packaging
• Manage source documentation, adverse event reporting, and maintain accurate records
• Communicate effectively with sponsors and CROs throughout the study lifecycle
• Prepare for and participate in site visits, including initiation and monitoring visits

QUALIFICATIONS

• 2+ years of experience as a Clinical Research Coordinator preferred
• Phlebotomy experience is required; EKG or other clinical experience a plus
• Strong organizational and documentation skills, with high attention to detail
• Familiarity with FDA, ICH-GCP, and electronic source documentation
• Strong communication skills and ability to work with diverse teams and patients
• Bachelor’s degree preferred but not required

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