Clinical Trial Associate
ICON · Burlington, Canada
Clinical OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Clinical Trial Associate role supporting sponsor-dedicated clinical research operations in a hybrid setting near Toronto. Responsibilities include trial coordination, regulatory documentation management, and cross-functional communication to ensure protocol compliance and successful trial execution.
What they're looking for
- Bachelor's degree in scientific or healthcare-related field
- Minimum two years supporting clinical trials
- 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
- 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 including study files and submissions
- Support preparation of study materials such as informed consent and case report forms
- Facilitate communication across cross-functional teams for trial execution
- Track and report clinical trial metrics and project milestones
Compensation$55,000–$67,000 CAD based on experience
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.