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 new 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