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 (Winnipeg)
🏢 ICON Strategic Solutions
📍 Winnipeg