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Clinical Trial Associate

ICON

Clinical Trial Associate role supporting the design, coordination, and administration of clinical trials in a hybrid setting. The position involves managing trial documentation, regulatory compliance, and cross-functional collaboration to advance innovative treatments.

Responsibilities

  • Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
  • Maintain and organize clinical trial documentation, study files, and regulatory submissions
  • Support preparation of study materials including informed consent and case report forms
  • Facilitate communication between cross-functional teams for smooth trial execution
  • Track and report clinical trial metrics and milestones

Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Prior experience or demonstrated interest in clinical research
  • Knowledge of clinical trial processes, regulations, and guidelines
  • Strong organizational and communication skills
  • Ability to work collaboratively with attention to detail
  • Willingness to travel approximately 10% as required
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