Job Description

We are currently looking for a detail-oriented and motivated Clinical Research Assistant with experience supporting clinical research studies in compliance with FDA regulations, Good Clinical Practice (GCP), and study protocols for a leading CRO in Miami, Florida.

Key Responsibilities

• Assisted with clinical research studies through data collection, analysis, and accurate record management
• Ensured compliance with study protocols, FDA regulations, and GCP guidelines
• Prepared and maintained source documentation for study visits
• Performed patient procedures including vitals, ECGs, and phlebotomy
• Completed accurate data entry and maintained research databases
• Processed and shipped laboratory specimens in accordance with protocol requirements
• Managed laboratory kit inventory and study materials
• Supported protocol training activities and study coordination tasks
• Maintained organised filing systems and completed administrative duties including scanning, copying, and document management
• Collaborated effectively with clinical and research teams to support study objectives

Requirements

• Clinical research support experience
• Highschool diploma or equivalent
• Data entry and documentation
• Regulatory compliance and GCP knowledge
• Strong organisational and communication skills
• Attention to detail and accuracy
• Ability to work independently and within a team environment

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