Join ICON Strategic Solutions as an Oncology Study Delivery Associate in Mississauga, Canada, in a hybrid work model that supports cutting-edge clinical trials. This role focuses on compliance and documentation for patient-centered research. You will be responsible for coordinating clinical trials, ensuring adherence to protocols, and supporting cross-functional team collaboration.

With a background in clinical research, your expertise will help maintain essential documentation and facilitate the development of current treatments for patients. Key Responsibilities:
Coordinate and administer clinical trials ensuring protocol compliance
Organize study files and regulatory documents
Prepare materials such as informed consent and case report forms
Work with teams to ensure smooth trial execution
Track and report on trial metrics and milestones Requirements:
Bachelor’s degree in a relevant field
Two years of clinical research experience needed
Familiarity with regulatory documentation
Oncology knowledge is essential
Excellent organizational and communication skills Contribute to valuable clinical research processes aimed at advancing oncology treatments through your role at ICON.

📌 Clinical Trials Associate At Icon Strategic Solutions Toronto
🏢 ICON Strategic Solutions
📍 Toronto