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Clinical Trial Associate

$55k - $67k per year

ICON

ICON is seeking a Clinical Trial Associate for a hybrid role in Mississauga to support clinical research operations within a sponsor-dedicated model. The position involves coordinating trial activities, managing documentation, and ensuring regulatory compliance across multiple concurrent studies.

Responsibilities

  • Coordinate and administer clinical trials while ensuring protocol and regulatory compliance
  • Maintain and organize clinical trial documentation, study files, and regulatory submissions
  • Prepare study-related materials including informed consent forms and case report forms
  • Facilitate cross-functional communication to support smooth trial execution
  • Track and report clinical trial metrics and milestone progress

Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum two years supporting clinical trials
  • Knowledge of clinical trial processes, regulations, and guidelines
  • Strong organizational and communication skills
  • Experience managing regulatory documentation for clinical trials
  • Ability to work collaboratively with attention to detail in fast-paced environment
  • Willingness to report to Mississauga office three days per week

Compensation: $55,000–$67,000 CAD base

Vacancy posted 4 days ago
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