Clinical Trial Associate
ICON · Burlington, Canada
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Trial Associate role supporting sponsor-dedicated clinical research projects in a hybrid work environment. Responsibilities include trial coordination, documentation management, regulatory compliance, and cross-functional collaboration to ensure successful study execution.
What they're looking for
- 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
- Experience managing regulatory documentation for clinical trials
- Excellent organizational and communication skills
- Ability to work collaboratively in fast-paced environment 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, study files, and regulatory submissions
- Support preparation of study materials including informed consent and case report forms
- Facilitate cross-functional communication to ensure smooth trial execution
- Track and report clinical trial metrics and milestones
Compensation$55,000–$66,000 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.