iconplc - Canada, Burlington, Remote work

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 ...

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...

Join ICON plc as a Clinical Research Associate II in Toronto/Burlington. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing new therapies. The role requires 2+ years of CRA experience and 60% travel. We offer competitive health insurance, retirement plan...

Join ICON plc, a global clinical research leader, as a CRA I in Burlington, Canada. Utilize your 2+ years of monitoring experience and ICH-GCP knowledge to conduct site visits and ensure trial excellence. This role offers competitive benefits and involves approximately 60% travel.

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate. This role requires 1-3+ years of monitoring experience, with oncology expertise preferred, and 70% travel. You will ensure trial compliance with ICH-GCP at sites across Canada, supported by comprehensive he...

Join ICON plc as a Senior Clinical Research Associate in Burlington, Canada. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires oncology monitoring experience and 60% travel. Enjoy health insurance, competitive retirement plans, and a supp...