Clinical Trial Associate
ICON · Burlington, Canada
Clinical OperationsFull-timeCompany career page
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Role summary
Clinical Trial Associate position at a large contract research organization, supporting sponsor-dedicated clinical research operations. The role involves trial coordination, documentation management, regulatory compliance, and cross-functional collaboration in a hybrid setup based in Mississauga.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum two years of clinical trial support experience
- Knowledge of clinical trial processes, regulations, and guidelines
- Experience managing regulatory documentation for clinical trials
- Excellent organizational and communication skills
- Ability to work collaboratively with attention to detail in fast-paced environment
- Willingness to report to Mississauga office 3 days per week
What you'll be doing
- 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 across cross-functional teams for smooth trial execution
- Track and report clinical trial metrics and milestones
Compensation$55,000–$67,000 CAD base
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.