Clinical Research Coordinator

X4 Life Sciences; Miami (FL); On-site; USD 55,000 - 75,000; Full time

Job summary

X4 Life Sciences in Orlando, FL is seeking an experienced Clinical Research Coordinator to join our expanding team. The ideal candidate will lead trial coordination, ensure regulatory compliance, and manage patient flow in clinical studies.

You will oversee informed consent, data collection, and coordination of visits, while mentoring junior staff and contributing to study planning and execution across sponsor-driven trials.

Qualifications

• 3+ years of experience as a Clinical Research Coordinator in a clinical research setting.
• Strong background in industry sponsored trials and working knowledge of ICH-GCP guidelines.
• Phlebotomy certification and clinical skills (vital signs, ECGs, specimen processing).
• Exceptional organizational skills, attention to detail, and ability to manage multiple studies simultaneously.
• Strong communication and leadership abilities with a collaborative approach to teamwork.

Responsibilities

• Oversee the coordination of multiple clinical trials in compliance with FDA regulations, ICH-GCP guidelines, and institutional policies
• Obtain and document informed consent from study participants in accordance with ethical and regulatory standards
• Perform clinical procedures, including phlebotomy, vital signs, ECGs, and specimen handling per study protocols
• Review, interpret, and manage laboratory results, ECGs, and other clinical data, ensuring timely investigator review and follow-up
• Identify, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) promptly to the Principal Investigator and sponsor
• Coordinate and manage patient scheduling, ensuring visits occur within protocol-specified windows
• Dispense investigational products per protocol, provide medication education, and monitor subject compliance and progress

Skills

Phlebotomy

Communication

Leadership

Clinical trial coordination

Job description

We are seeking an experienced Clinical Research Coordinator to join an expanding research team in Orlando, FL. The ideal candidate will bring advanced expertise in clinical trial coordination, regulatory compliance, and patient management, as well as leadership in supporting junior staff and contributing to study planning and execution.

Key Responsibilities

• Oversee the coordination of multiple clinical trials in compliance with FDA regulations, ICH-GCP guidelines, and institutional policies
• Obtain and document informed consent from study participants in accordance with ethical and regulatory standards
• Perform clinical procedures, including phlebotomy, vital signs, ECGs, and specimen handling per study protocols
• Review, interpret, and manage laboratory results, ECGs, and other clinical data, ensuring timely investigator review and follow-up
• Identify, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) promptly to the Principal Investigator and sponsor
• Coordinate and manage patient scheduling, ensuring visits occur within protocol-specified windows
• Dispense investigational products per protocol, provide medication education, and monitor subject compliance and progress

Requirements:

• 3+ years of experience as a Clinical Research Coordinator in a clinical research setting
• Strong background in industry sponsored trials and working knowledge of ICH-GCP guidelines
• Phlebotomy certification and clinical skills (vital signs, ECGs, specimen processing)
• Exceptional organizational skills, attention to detail, and ability to manage multiple studies simultaneously
• Strong communication and leadership abilities with a collaborative approach to teamwork

If you are an experienced clinical research professional passionate about advancing medical knowledge and improving patient care, we invite you to apply. Join our Miami-based research team and contribute to innovative, life-changing clinical studies that make a real impact.