iconplc - Canada, Remote work

Senior CRA opportunity in Montreal, Canada, with ICON Plc, specializing in Medical Device and Cardiology trials. You will oversee site monitoring, ensure GCP and regulatory compliance, and manage multiple projects. Requires a Bachelor’s in a scientific field, extensive CRA experience, and strong ...

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...

Senior Clinical Research Associate sought in Montreal, Toronto, or Ontario. Lead monitoring for clinical trials, ensuring GCP compliance and data integrity across multiple sites. Requires bilingual (French/English) expertise, 60% travel, and strong site management skills. Benefits include health ...

Join ICON as a Senior CRA in Montreal, Canada, and lead Oncology study monitoring in a sponsor-dedicated role. Leverage your ICH-GCP expertise and medical/science degree to ensure patient safety and data quality. Enjoy 60% travel, competitive benefits including health insurance and retirement pla...

Join ICON plc as a Clinical Research Associate in Montreal, Canada. Monitor multi-therapeutic area studies in a sponsor-dedicated program, focusing on Oncology. Leverage your ICH-GCP expertise and medical knowledge to ensure patient safety and data quality. Enjoy competitive benefits, including h...

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 ...

Join ICON plc as an **Evidence Delivery Specialist** in Burlington, Canada. You will ensure inspection-readiness by managing TMF/Master File QC, customizing Expected Document Lists, and collaborating with CROs. Ideal for candidates with a Bachelor’s in life sciences, GCP/ICH knowledge, and strong...

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 Clinical Research Associate II in Montreal. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing new therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance,...