Clinical Data Coordinator

We are seeking a detail-oriented Clinical Data Coordinator to support a leading clinical research organisation in Miami, Florida. This position involves accurate data processing, documentation, and study record management, maintaining confidential participant data, completing study-related data entry tasks, and ensuring compliance with clinical research guidelines and internal procedures.

This position is 37.5-40 hours per week, and a 6 month rolling contract with high likelihood of extension.

• Accurately enter and review clinical study data
• Maintain organised and confidential participant records
• Complete data entry for paper and electronic case report forms
• Monitor data completion and resolve discrepancies as needed
• Support data quality checks and query resolution
• Follow study protocols, SOPs, and regulatory guidelines
• Complete required system and sponsor training

• High school diploma or equivalent
• Previous data entry or administrative experience preferred
• Strong attention to detail and organisational skills
• Proficiency with Microsoft Office and database systems
• Ability to communicate professionally and work collaboratively
• Experience in a clinical or research environment preferred
• Familiarity with GCP/ICH guidelines is an advantage