Job Description

Clinical Research Coordinator overseeing day-to-day operations of clinical trials at a Florida-based site. Manages study execution, participant enrollment, protocol compliance, and supervises team members while liaising with research stakeholders.

Responsibilities

• Conduct and oversee multiple concurrent clinical trials of varying complexity with patient and volunteer subjects
• Complete study-required documentation ensuring protocol adherence, participant safety and informed consent
• Lead recruitment, enrollment, and retention efforts for study participants across site operations
• Supervise and mentor junior coordinators and administrative staff on study procedures
• Communicate with research monitors, interdepartmental teams, and external stakeholders regarding trial progress

Requirements

• Bachelor's degree or equivalent formal qualification
• 0-5 years relevant experience; minimum 1 year leadership responsibility
• Proficiency in FDA Good Clinical Practices and ICH Guidelines
• Strong organizational skills managing multiple concurrent tasks
• Advanced communication and staff supervision abilities
• Knowledge of records management principles and eTMF systems
• Ability to lift 40 lbs; frequent domestic and international travel

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