Clinical Research Associate – Oncology Focus

Join ICON plc as a Clinical Research Associate specializing in Oncology in Montreal. Deliver exceptional clinical trial monitoring while ensuring patient safety and study compliance.
Your role will center on the management of clinical trial operations. You will ensure high-quality monitoring, coordinate activities effectively, and maintain study documentation. This position emphasizes strong collaboration with site staff and stakeholders within an inclusive environment.
Key Responsibilities:
• Coordinate study setup and independent monitoring tasks
• Respond to sponsor-generated queries promptly
• Build strong relationships with clinical investigators
• Ensure compliance with all regulatory requirements
Requirements:
• Degree in medicine, science, or equivalent
• Familiarity with ICH-GCP guidelines
• Proven experience in Oncology study monitoring
• Strong English communication skills, both written and verbal
• Ability to travel as required, about 60%...