Join ICON Strategic Solutions as an Oncology Study Delivery Associate in Mississauga, Canada, in a hybrid work model that supports creative 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.
#J-18808-Ljbffr

📌 Clinical Trials Associate at ICON Strategic Solutions (Ontario)
🏢 ICON Strategic Solutions
📍 Ontario