Clinical Research Coordinator

Role Description

This is a full-time on-site role for a Clinical Research Coordinator located in North Miami Beach, FL. The Clinical Research Coordinator will manage day-to-day clinical trial activities, including obtaining informed consent from study participants, adhering to research protocols, and ensuring compliance with regulatory requirements. Responsibilities also include coordinating clinical trials, managing study documentation, and ensuring accurate data collection and reporting.

Qualifications

• Experience with Informed Consent, understanding and obtaining consent from participants
• Knowledge of research Protocols, including development and adherence to study plans
• Clinical Research Experience, with a background in managing and coordinating studies
• Proficiency in managing Clinical Trials, including data collection, reporting, and compliance
• Strong organizational and communication skills
• Ability to work on-site in North Miami Beach, FL
• Bachelor's degree in a related field such as Life Sciences, Nursing, or a related discipline is preferred