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 in a hybrid setting near Toronto. Responsibilities include trial coordination, documentation management, regulatory compliance, and cross-functional communication to ensure successful study execution.
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
- Willingness to report to Mississauga office three 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 regulatory submissions
- Support preparation of study materials such as informed consent and case report forms
- Facilitate communication between cross-functional teams during trial execution
- Track and report clinical trial metrics and project 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.