Sr CRA

Sr CRA role focused on monitoring Oncology trials in Montreal. Responsibilities include independently coordinating activities for setup and monitoring of studies, maintaining accurate study status reports and documentation, efficiently handling sponsor queries, and contributing to study cost efficiency. You will prepare and review study documentation and feasibility studies for proposals, develop strong, collaborative relationships with clinical investigators and site staff, and ensure patient safety by complying with ICON procedures, protocols, and regulatory requirements. The ideal candidate has clinical trial monitoring experience, knowledge of ICH-GCP guidelines, excellent English communication, and willingness to travel (~60%). Bilingual French/English skills are present in the description. Employment with ICON is contingent upon right to work in the country. Education required: university degree in medicine, science, or equivalent; competencies in medical data review and regulatory compliance; able to interact with stakeholders and manage queries. Location-based travel and a Montreal office/onsite setup are expected.