Clinical Trial Associate
$55k - $67k per yearICON
Clinical Trial Associate position supporting sponsor-dedicated clinical research initiatives in a hybrid model. The role involves coordinating trial administration, managing regulatory documentation, and collaborating with cross-functional teams to ensure protocol compliance and successful trial execution.
Responsibilities
- 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 cross-functional team communication to ensure smooth trial execution
- Track and report clinical trial metrics and milestones
Requirements
- 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 in fast-paced environment with attention to detail
- Willingness to report to Mississauga office three days per week
Compensation: $55,000–$67,000 CAD base
Vacancy posted 7 days ago
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