Job Description

Clinical Research Coordinator role at ICON in McComb, Mississippi, involving coordination and execution of clinical trials, regulatory compliance, and participant management. The position requires a bachelor's degree in a scientific or healthcare field and prior clinical research experience.

Responsibilities

• Facilitate coordination and execution of clinical research studies including participant recruitment and enrollment
• Collaborate with principal investigators, study sponsors, and regulatory authorities on protocol and compliance matters
• Collect, maintain, and document clinical trial data including adverse events and protocol deviations
• Manage study documentation such as informed consent forms, case report forms, and regulatory submissions
• Provide support and education to study participants throughout the research process

Requirements

• Bachelor's degree in relevant scientific or healthcare-related field
• Previous experience in clinical research or healthcare settings
• Knowledge of FDA/EMA regulations, ICH-GCP guidelines, and HIPAA
• Strong organizational, communication, and interpersonal skills
• Detail-oriented with ability to manage multiple priorities simultaneously
• Legal right to work in the United States

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