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 complianceOrganize study files and regulatory documentsPrepare materials such as informed consent and case report formsWork with teams to ensure smooth trial executionTrack and report on trial metrics and milestonesRequirements:Bachelor's degree in a relevant fieldTwo years of clinical research experience neededFamiliarity with regulatory documentationOncology knowledge is essentialExcellent organizational and communication skillsContribute 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