iconplc - Canada, IT - Software Development

Join ICON as a Clinical Research Associate in Western Canada (Alberta, Vancouver, Burlington). Monitor Oncology studies in a sponsor-dedicated program, ensuring patient safety and regulatory compliance. Requires a science degree, ICH-GCP knowledge, and Oncology monitoring experience. Enjoy compet...

Join ICON plc as an Evidence Delivery Specialist in Burlington, Canada. You will manage sponsor oversight, maintain inspection-readiness, and coordinate TMF/Master File QC. Ideal for candidates with a Bachelor's in life sciences, GCP/ICH knowledge, and strong collaboration skills. Enjoy benefits ...

Senior Clinical Research Associate – home-based across Canada. Join ICON, a world-leading clinical research organization, to monitor trial progress ensuring ICH-GCP and regulatory compliance. Ideal for candidates with a scientific degree, 1-3+ years of monitoring experience, and 70% travel flexib...

Global Study Manager role at ICON in Canada: Lead and manage complex projects in the pharmaceutical or biotech industry. Requires a Bachelor’s degree in a scientific discipline, extensive project management experience, and strong leadership skills. Drive cross-functional teams, develop project pl...

Join ICON plc as a Senior Statistical Programmer II in Montreal (remote). Utilize your advanced SAS and R-Shiny skills to analyze clinical trial data, ensuring statistical integrity. This role offers competitive benefits and a chance to shape the future of clinical development within a global lea...