Elevate your career as a Clinical Trial Associate with ICON in Mississauga, Ontario. This hybrid role focuses on oncology research, trial coordination, and regulatory compliance. In this energetic position, you will support clinical trial design and execution while ensuring regulations are met.
Collaborate closely with teams and stakeholders to deliver quality research outcomes. Your contributions will assist in advancing innovative therapies and manage complex medical data to drive clinical excellence. Key Responsibilities:
Coordinate and administer clinical trials to ensure compliance
Organize clinical trial documentation and essential study files
Prepare study-related materials, including consent forms
Facilitate communication within cross-functional teams
Track and report clinical trial metrics and milestones Requirements:
Bachelor’s degree in a scientific or healthcare field
Experience or solid interest in clinical research
Knowledge of clinical trial regulations and guidelines
Strong organizational and communication skills
Experience in oncology studies required Join ICON to contribute to pioneering clinical research and advance your qualified journey.