Clinical Research Coordinator Job at ICON, Mississippi

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  • ICON
  • Mississippi

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

Job Tags

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